Canonical Allele Identifier: CA346820153

Gene: NRXN1

Linked Data

• MyVariant Identifiers: chr2:g.50282153C>A (hg19) ; chr2:g.50055015C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.50055015C>A , CM000664.2:g.50055015C>A	GRCh38
NC_000002.11:g.50282153C>A , CM000664.1:g.50282153C>A	GRCh37
NC_000002.10:g.50135657C>A	NCBI36
NG_011878.1:g.982522G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000401669.7:c.3748G>T MANE Select	ENSP00000385017.2:p.Ala1250Ser
ENST00000637889.1:n.915G>T
ENST00000637906.1:c.606-1425G>T	ENSP00000490198.1:n.606-1425G>T
ENST00000342183.9:c.614-1425G>T	ENSP00000341184.5:n.614-1425G>T
ENST00000401669.6:c.3748G>T	ENSP00000385017.2:p.Ala1250Ser
ENST00000401710.5:c.643G>T	ENSP00000385580.2:p.Ala215Ser
ENST00000404971.5:c.3868G>T	ENSP00000385142.1:p.Ala1290Ser
ENST00000405472.7:c.3712G>T	ENSP00000434015.2:p.Ala1238Ser
ENST00000406316.6:c.3719-1425G>T	ENSP00000384311.2:n.3719-1425G>T
ENST00000611589.4:c.-119-1425G>T	ENSP00000483634.1:n.-119-1425G>T
ENST00000625672.2:c.3724G>T	ENSP00000485887.1:p.Ala1242Ser
ENST00000628364.2:c.643G>T	ENSP00000485815.1:p.Ala215Ser
ENST00000630543.2:c.3724G>T	ENSP00000486879.1:p.Ala1242Ser
ENST00000635264.1:n.557G>T
NM_001135659.1:c.3868G>T	NP_001129131.1:p.Ala1290Ser
NM_004801.4:c.3719-1425G>T	NP_004792.1:n.3719-1425G>T
NM_138735.2:c.614-1425G>T	NP_620072.1:n.614-1425G>T
XM_005264642.2:c.3769G>T	XP_005264699.1:p.Ala1257Ser
XM_005264643.2:c.3724G>T	XP_005264700.1:p.Ala1242Ser
XM_006712137.2:c.3740-1425G>T	XP_006712200.1:n.3740-1425G>T
XM_006712140.2:c.3769G>T	XP_006712203.1:p.Ala1257Ser
XM_011533167.1:c.3769G>T	XP_011531469.1:p.Ala1257Ser
XM_011533168.1:c.3766G>T	XP_011531470.1:p.Ala1256Ser
XM_011533169.1:c.3757G>T	XP_011531471.1:p.Ala1253Ser
XM_011533170.1:c.3751G>T	XP_011531472.1:p.Ala1251Ser
XM_011533171.1:c.3748G>T	XP_011531473.1:p.Ala1250Ser
XM_011533172.1:c.3742G>T	XP_011531474.1:p.Ala1248Ser
XM_011533173.1:c.3739G>T	XP_011531475.1:p.Ala1247Ser
XM_011533174.1:c.3724G>T	XP_011531476.1:p.Ala1242Ser
XM_011533175.1:c.3712G>T	XP_011531477.1:p.Ala1238Ser
XM_011533176.1:c.3709G>T	XP_011531478.1:p.Ala1237Ser
XM_011533177.1:c.3740-1425G>T	XP_011531479.1:n.3740-1425G>T
XM_011533178.1:c.3679G>T	XP_011531480.1:p.Ala1227Ser
XM_011533179.1:c.3695-1425G>T	XP_011531481.1:n.3695-1425G>T
XM_011533180.1:c.3769G>T	XP_011531482.1:p.Ala1257Ser
XM_011533181.1:c.2974G>T	XP_011531483.1:p.Ala992Ser
XM_011533182.1:c.2929G>T	XP_011531484.1:p.Ala977Ser
XM_011533183.1:c.2902G>T	XP_011531485.1:p.Ala968Ser
XM_011533184.1:c.2809G>T	XP_011531486.1:p.Ala937Ser
NM_001135659.2:c.3868G>T	NP_001129131.1:p.Ala1290Ser
NM_001330077.1:c.3724G>T	NP_001317006.1:p.Ala1242Ser
NM_001330078.1:c.3748G>T	NP_001317007.1:p.Ala1250Ser
NM_001330082.1:c.3724G>T	NP_001317011.1:p.Ala1242Ser
NM_001330083.1:c.3653-1425G>T	NP_001317012.1:n.3653-1425G>T
NM_001330084.1:c.3682G>T	NP_001317013.1:p.Ala1228Ser
NM_001330085.1:c.3721G>T	NP_001317014.1:p.Ala1241Ser
NM_001330086.1:c.3748G>T	NP_001317015.1:p.Ala1250Ser
NM_001330087.1:c.3608-1425G>T	NP_001317016.1:n.3608-1425G>T
NM_001330088.1:c.3638-1425G>T	NP_001317017.1:n.3638-1425G>T
NM_001330091.1:c.643G>T	NP_001317020.1:p.Ala215Ser
NM_001330092.1:c.643G>T	NP_001317021.1:p.Ala215Ser
NM_001330093.1:c.3745G>T	NP_001317022.1:p.Ala1249Ser
NM_001330094.1:c.3736G>T	NP_001317023.1:p.Ala1246Ser
NM_001330095.1:c.3668-1425G>T	NP_001317024.1:n.3668-1425G>T
NM_001330096.1:c.3608-1425G>T	NP_001317025.1:n.3608-1425G>T
NM_001330097.1:c.614-1425G>T	NP_001317026.1:n.614-1425G>T
NM_004801.5:c.3719-1425G>T	NP_004792.1:n.3719-1425G>T
NM_138735.4:c.614-1425G>T	NP_620072.1:n.614-1425G>T
XM_005264642.4:c.3769G>T	XP_005264699.1:p.Ala1257Ser
XM_006712137.4:c.3740-1425G>T	XP_006712200.1:n.3740-1425G>T
XM_006712140.4:c.3796G>T	XP_006712203.2:p.Ala1266Ser
XM_011533167.3:c.3769G>T	XP_011531469.1:p.Ala1257Ser
XM_011533172.3:c.3742G>T	XP_011531474.1:p.Ala1248Ser
XM_011533175.3:c.3712G>T	XP_011531477.1:p.Ala1238Ser
XM_011533177.3:c.3740-1425G>T	XP_011531479.1:n.3740-1425G>T
XM_011533178.3:c.3679G>T	XP_011531480.1:p.Ala1227Ser
XM_011533180.3:c.3769G>T	XP_011531482.1:p.Ala1257Ser
XM_011533183.2:c.2902G>T	XP_011531485.1:p.Ala968Ser
XM_017005303.2:c.3796G>T	XP_016860792.1:p.Ala1266Ser
XM_017005304.2:c.3793G>T	XP_016860793.1:p.Ala1265Ser
XM_017005305.2:c.3796G>T	XP_016860794.1:p.Ala1266Ser
XM_017005306.2:c.3784G>T	XP_016860795.1:p.Ala1262Ser
XM_017005307.2:c.3778G>T	XP_016860796.1:p.Ala1260Ser
XM_017005308.2:c.3775G>T	XP_016860797.1:p.Ala1259Ser
XM_017005309.2:c.3769G>T	XP_016860798.1:p.Ala1257Ser
XM_017005310.2:c.3766G>T	XP_016860799.1:p.Ala1256Ser
XM_017005311.2:c.3751G>T	XP_016860800.1:p.Ala1251Ser
XM_017005314.2:c.3736G>T	XP_016860803.1:p.Ala1246Ser
XM_017005315.2:c.3742G>T	XP_016860804.1:p.Ala1248Ser
XM_017005316.2:c.3733G>T	XP_016860805.1:p.Ala1245Ser
XM_017005318.2:c.3724G>T	XP_016860807.1:p.Ala1242Ser
XM_017005320.2:c.3721G>T	XP_016860809.1:p.Ala1241Ser
XM_017005321.2:c.3767-1425G>T	XP_016860810.1:n.3767-1425G>T
XM_017005322.2:c.3767-1425G>T	XP_016860811.1:n.3767-1425G>T
XM_017005324.2:c.3713-1425G>T	XP_016860813.1:n.3713-1425G>T
XM_017005325.2:c.3713-1425G>T	XP_016860814.1:n.3713-1425G>T
XM_017005326.2:c.3701-1425G>T	XP_016860815.1:n.3701-1425G>T
XM_017005327.2:c.3695-1425G>T	XP_016860816.1:n.3695-1425G>T
XM_017005329.2:c.3796G>T	XP_016860818.1:p.Ala1266Ser
XM_017005334.2:c.2836G>T	XP_016860823.1:p.Ala946Ser
NM_001330078.2:c.3748G>T MANE Select	NP_001317007.1:p.Ala1250Ser
NM_001135659.3:c.3868G>T	NP_001129131.1:p.Ala1290Ser
NM_001330077.2:c.3724G>T	NP_001317006.1:p.Ala1242Ser
NM_001330082.2:c.3724G>T	NP_001317011.1:p.Ala1242Ser
NM_001330083.2:c.3653-1425G>T	NP_001317012.1:n.3653-1425G>T
NM_001330084.2:c.3682G>T	NP_001317013.1:p.Ala1228Ser
NM_001330085.2:c.3721G>T	NP_001317014.1:p.Ala1241Ser
NM_001330086.2:c.3748G>T	NP_001317015.1:p.Ala1250Ser
NM_001330087.2:c.3608-1425G>T	NP_001317016.1:n.3608-1425G>T
NM_001330088.2:c.3638-1425G>T	NP_001317017.1:n.3638-1425G>T
NM_001330091.2:c.643G>T	NP_001317020.1:p.Ala215Ser
NM_001330092.2:c.643G>T	NP_001317021.1:p.Ala215Ser
NM_001330093.2:c.3745G>T	NP_001317022.1:p.Ala1249Ser
NM_001330094.2:c.3736G>T	NP_001317023.1:p.Ala1246Ser
NM_001330095.2:c.3668-1425G>T	NP_001317024.1:n.3668-1425G>T
NM_001330096.2:c.3608-1425G>T	NP_001317025.1:n.3608-1425G>T
NM_001330097.2:c.614-1425G>T	NP_001317026.1:n.614-1425G>T
NM_004801.6:c.3719-1425G>T	NP_004792.1:n.3719-1425G>T
NM_138735.5:c.614-1425G>T	NP_620072.1:n.614-1425G>T