Canonical Allele Identifier: CA346820187
Gene: NRXN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.50055032T>G , CM000664.2:g.50055032T>G GRCh38
NC_000002.11:g.50282170T>G , CM000664.1:g.50282170T>G GRCh37
NC_000002.10:g.50135674T>G NCBI36
NG_011878.1:g.982505A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000401669.7:c.3731A>C MANE Select ENSP00000385017.2:p.Asn1244Thr
ENST00000637889.1:n.898A>C
ENST00000637906.1:c.606-1442A>C ENSP00000490198.1:n.606-1442A>C
ENST00000342183.9:c.614-1442A>C ENSP00000341184.5:n.614-1442A>C
ENST00000401669.6:c.3731A>C ENSP00000385017.2:p.Asn1244Thr
ENST00000401710.5:c.626A>C ENSP00000385580.2:p.Asn209Thr
ENST00000404971.5:c.3851A>C ENSP00000385142.1:p.Asn1284Thr
ENST00000405472.7:c.3695A>C ENSP00000434015.2:p.Asn1232Thr
ENST00000406316.6:c.3719-1442A>C ENSP00000384311.2:n.3719-1442A>C
ENST00000611589.4:c.-119-1442A>C ENSP00000483634.1:n.-119-1442A>C
ENST00000625672.2:c.3707A>C ENSP00000485887.1:p.Asn1236Thr
ENST00000628364.2:c.626A>C ENSP00000485815.1:p.Asn209Thr
ENST00000630543.2:c.3707A>C ENSP00000486879.1:p.Asn1236Thr
ENST00000635264.1:n.540A>C
NM_001135659.1:c.3851A>C NP_001129131.1:p.Asn1284Thr
NM_004801.4:c.3719-1442A>C NP_004792.1:n.3719-1442A>C
NM_138735.2:c.614-1442A>C NP_620072.1:n.614-1442A>C
XM_005264642.2:c.3752A>C XP_005264699.1:p.Asn1251Thr
XM_005264643.2:c.3707A>C XP_005264700.1:p.Asn1236Thr
XM_006712137.2:c.3740-1442A>C XP_006712200.1:n.3740-1442A>C
XM_006712140.2:c.3752A>C XP_006712203.1:p.Asn1251Thr
XM_011533167.1:c.3752A>C XP_011531469.1:p.Asn1251Thr
XM_011533168.1:c.3749A>C XP_011531470.1:p.Asn1250Thr
XM_011533169.1:c.3740A>C XP_011531471.1:p.Asn1247Thr
XM_011533170.1:c.3734A>C XP_011531472.1:p.Asn1245Thr
XM_011533171.1:c.3731A>C XP_011531473.1:p.Asn1244Thr
XM_011533172.1:c.3725A>C XP_011531474.1:p.Asn1242Thr
XM_011533173.1:c.3722A>C XP_011531475.1:p.Asn1241Thr
XM_011533174.1:c.3707A>C XP_011531476.1:p.Asn1236Thr
XM_011533175.1:c.3695A>C XP_011531477.1:p.Asn1232Thr
XM_011533176.1:c.3692A>C XP_011531478.1:p.Asn1231Thr
XM_011533177.1:c.3740-1442A>C XP_011531479.1:n.3740-1442A>C
XM_011533178.1:c.3662A>C XP_011531480.1:p.Asn1221Thr
XM_011533179.1:c.3695-1442A>C XP_011531481.1:n.3695-1442A>C
XM_011533180.1:c.3752A>C XP_011531482.1:p.Asn1251Thr
XM_011533181.1:c.2957A>C XP_011531483.1:p.Asn986Thr
XM_011533182.1:c.2912A>C XP_011531484.1:p.Asn971Thr
XM_011533183.1:c.2885A>C XP_011531485.1:p.Asn962Thr
XM_011533184.1:c.2792A>C XP_011531486.1:p.Asn931Thr
NM_001135659.2:c.3851A>C NP_001129131.1:p.Asn1284Thr
NM_001330077.1:c.3707A>C NP_001317006.1:p.Asn1236Thr
NM_001330078.1:c.3731A>C NP_001317007.1:p.Asn1244Thr
NM_001330082.1:c.3707A>C NP_001317011.1:p.Asn1236Thr
NM_001330083.1:c.3653-1442A>C NP_001317012.1:n.3653-1442A>C
NM_001330084.1:c.3665A>C NP_001317013.1:p.Asn1222Thr
NM_001330085.1:c.3704A>C NP_001317014.1:p.Asn1235Thr
NM_001330086.1:c.3731A>C NP_001317015.1:p.Asn1244Thr
NM_001330087.1:c.3608-1442A>C NP_001317016.1:n.3608-1442A>C
NM_001330088.1:c.3638-1442A>C NP_001317017.1:n.3638-1442A>C
NM_001330091.1:c.626A>C NP_001317020.1:p.Asn209Thr
NM_001330092.1:c.626A>C NP_001317021.1:p.Asn209Thr
NM_001330093.1:c.3728A>C NP_001317022.1:p.Asn1243Thr
NM_001330094.1:c.3719A>C NP_001317023.1:p.Asn1240Thr
NM_001330095.1:c.3668-1442A>C NP_001317024.1:n.3668-1442A>C
NM_001330096.1:c.3608-1442A>C NP_001317025.1:n.3608-1442A>C
NM_001330097.1:c.614-1442A>C NP_001317026.1:n.614-1442A>C
NM_004801.5:c.3719-1442A>C NP_004792.1:n.3719-1442A>C
NM_138735.4:c.614-1442A>C NP_620072.1:n.614-1442A>C
XM_005264642.4:c.3752A>C XP_005264699.1:p.Asn1251Thr
XM_006712137.4:c.3740-1442A>C XP_006712200.1:n.3740-1442A>C
XM_006712140.4:c.3779A>C XP_006712203.2:p.Asn1260Thr
XM_011533167.3:c.3752A>C XP_011531469.1:p.Asn1251Thr
XM_011533172.3:c.3725A>C XP_011531474.1:p.Asn1242Thr
XM_011533175.3:c.3695A>C XP_011531477.1:p.Asn1232Thr
XM_011533177.3:c.3740-1442A>C XP_011531479.1:n.3740-1442A>C
XM_011533178.3:c.3662A>C XP_011531480.1:p.Asn1221Thr
XM_011533180.3:c.3752A>C XP_011531482.1:p.Asn1251Thr
XM_011533183.2:c.2885A>C XP_011531485.1:p.Asn962Thr
XM_017005303.2:c.3779A>C XP_016860792.1:p.Asn1260Thr
XM_017005304.2:c.3776A>C XP_016860793.1:p.Asn1259Thr
XM_017005305.2:c.3779A>C XP_016860794.1:p.Asn1260Thr
XM_017005306.2:c.3767A>C XP_016860795.1:p.Asn1256Thr
XM_017005307.2:c.3761A>C XP_016860796.1:p.Asn1254Thr
XM_017005308.2:c.3758A>C XP_016860797.1:p.Asn1253Thr
XM_017005309.2:c.3752A>C XP_016860798.1:p.Asn1251Thr
XM_017005310.2:c.3749A>C XP_016860799.1:p.Asn1250Thr
XM_017005311.2:c.3734A>C XP_016860800.1:p.Asn1245Thr
XM_017005314.2:c.3719A>C XP_016860803.1:p.Asn1240Thr
XM_017005315.2:c.3725A>C XP_016860804.1:p.Asn1242Thr
XM_017005316.2:c.3716A>C XP_016860805.1:p.Asn1239Thr
XM_017005318.2:c.3707A>C XP_016860807.1:p.Asn1236Thr
XM_017005320.2:c.3704A>C XP_016860809.1:p.Asn1235Thr
XM_017005321.2:c.3767-1442A>C XP_016860810.1:n.3767-1442A>C
XM_017005322.2:c.3767-1442A>C XP_016860811.1:n.3767-1442A>C
XM_017005324.2:c.3713-1442A>C XP_016860813.1:n.3713-1442A>C
XM_017005325.2:c.3713-1442A>C XP_016860814.1:n.3713-1442A>C
XM_017005326.2:c.3701-1442A>C XP_016860815.1:n.3701-1442A>C
XM_017005327.2:c.3695-1442A>C XP_016860816.1:n.3695-1442A>C
XM_017005329.2:c.3779A>C XP_016860818.1:p.Asn1260Thr
XM_017005334.2:c.2819A>C XP_016860823.1:p.Asn940Thr
NM_001330078.2:c.3731A>C MANE Select NP_001317007.1:p.Asn1244Thr
NM_001135659.3:c.3851A>C NP_001129131.1:p.Asn1284Thr
NM_001330077.2:c.3707A>C NP_001317006.1:p.Asn1236Thr
NM_001330082.2:c.3707A>C NP_001317011.1:p.Asn1236Thr
NM_001330083.2:c.3653-1442A>C NP_001317012.1:n.3653-1442A>C
NM_001330084.2:c.3665A>C NP_001317013.1:p.Asn1222Thr
NM_001330085.2:c.3704A>C NP_001317014.1:p.Asn1235Thr
NM_001330086.2:c.3731A>C NP_001317015.1:p.Asn1244Thr
NM_001330087.2:c.3608-1442A>C NP_001317016.1:n.3608-1442A>C
NM_001330088.2:c.3638-1442A>C NP_001317017.1:n.3638-1442A>C
NM_001330091.2:c.626A>C NP_001317020.1:p.Asn209Thr
NM_001330092.2:c.626A>C NP_001317021.1:p.Asn209Thr
NM_001330093.2:c.3728A>C NP_001317022.1:p.Asn1243Thr
NM_001330094.2:c.3719A>C NP_001317023.1:p.Asn1240Thr
NM_001330095.2:c.3668-1442A>C NP_001317024.1:n.3668-1442A>C
NM_001330096.2:c.3608-1442A>C NP_001317025.1:n.3608-1442A>C
NM_001330097.2:c.614-1442A>C NP_001317026.1:n.614-1442A>C
NM_004801.6:c.3719-1442A>C NP_004792.1:n.3719-1442A>C
NM_138735.5:c.614-1442A>C NP_620072.1:n.614-1442A>C