Canonical Allele Identifier: CA288974

Gene: NRXN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.50053331C>T , CM000664.2:g.50053331C>T	GRCh38
NC_000002.11:g.50280469C>T , CM000664.1:g.50280469C>T	GRCh37
NC_000002.10:g.50133973C>T	NCBI36
NG_011878.1:g.984206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401669.7:c.4068G>A MANE Select	ENSP00000385017.2:p.Thr1356=
ENST00000637889.1:n.1235G>A
ENST00000637906.1:c.865G>A	ENSP00000490198.1:n.865G>A
ENST00000342183.9:c.873G>A	ENSP00000341184.5:p.Thr291=
ENST00000401669.6:c.4068G>A	ENSP00000385017.2:p.Thr1356=
ENST00000401710.5:c.963G>A	ENSP00000385580.2:p.Thr321=
ENST00000404971.5:c.4188G>A	ENSP00000385142.1:p.Thr1396=
ENST00000405472.7:c.4032G>A	ENSP00000434015.2:p.Thr1344=
ENST00000406316.6:c.3978G>A	ENSP00000384311.2:p.Thr1326=
ENST00000611589.4:c.141G>A	ENSP00000483634.1:p.Thr47=
ENST00000625672.2:c.4044G>A	ENSP00000485887.1:p.Thr1348=
ENST00000628364.2:c.963G>A	ENSP00000485815.1:p.Thr321=
ENST00000630543.2:c.4044G>A	ENSP00000486879.1:p.Thr1348=
ENST00000635264.1:n.877G>A
NM_001135659.1:c.4188G>A	NP_001129131.1:p.Thr1396=
NM_004801.4:c.3978G>A	NP_004792.1:p.Thr1326=
NM_138735.2:c.873G>A	NP_620072.1:p.Thr291=
XM_005264642.2:c.4089G>A	XP_005264699.1:p.Thr1363=
XM_005264643.2:c.4044G>A	XP_005264700.1:p.Thr1348=
XM_006712137.2:c.3999G>A	XP_006712200.1:p.Thr1333=
XM_006712140.2:c.4089G>A	XP_006712203.1:p.Thr1363=
XM_011533167.1:c.4089G>A	XP_011531469.1:p.Thr1363=
XM_011533168.1:c.4086G>A	XP_011531470.1:p.Thr1362=
XM_011533169.1:c.4077G>A	XP_011531471.1:p.Thr1359=
XM_011533170.1:c.4071G>A	XP_011531472.1:p.Thr1357=
XM_011533171.1:c.4068G>A	XP_011531473.1:p.Thr1356=
XM_011533172.1:c.4062G>A	XP_011531474.1:p.Thr1354=
XM_011533173.1:c.4059G>A	XP_011531475.1:p.Thr1353=
XM_011533174.1:c.4044G>A	XP_011531476.1:p.Thr1348=
XM_011533175.1:c.4032G>A	XP_011531477.1:p.Thr1344=
XM_011533176.1:c.4029G>A	XP_011531478.1:p.Thr1343=
XM_011533177.1:c.3999G>A	XP_011531479.1:p.Thr1333=
XM_011533178.1:c.3999G>A	XP_011531480.1:p.Thr1333=
XM_011533179.1:c.3954G>A	XP_011531481.1:p.Thr1318=
XM_011533180.1:c.4089G>A	XP_011531482.1:p.Thr1363=
XM_011533181.1:c.3294G>A	XP_011531483.1:p.Thr1098=
XM_011533182.1:c.3249G>A	XP_011531484.1:p.Thr1083=
XM_011533183.1:c.3222G>A	XP_011531485.1:p.Thr1074=
XM_011533184.1:c.3129G>A	XP_011531486.1:p.Thr1043=
NM_001135659.2:c.4188G>A	NP_001129131.1:p.Thr1396=
NM_001330077.1:c.4044G>A	NP_001317006.1:p.Thr1348=
NM_001330078.1:c.4068G>A	NP_001317007.1:p.Thr1356=
NM_001330082.1:c.4044G>A	NP_001317011.1:p.Thr1348=
NM_001330083.1:c.3912G>A	NP_001317012.1:p.Thr1304=
NM_001330084.1:c.4002G>A	NP_001317013.1:p.Thr1334=
NM_001330085.1:c.4041G>A	NP_001317014.1:p.Thr1347=
NM_001330086.1:c.4068G>A	NP_001317015.1:p.Thr1356=
NM_001330087.1:c.3867G>A	NP_001317016.1:p.Thr1289=
NM_001330088.1:c.3897G>A	NP_001317017.1:p.Thr1299=
NM_001330091.1:c.963G>A	NP_001317020.1:p.Thr321=
NM_001330092.1:c.963G>A	NP_001317021.1:p.Thr321=
NM_001330093.1:c.4065G>A	NP_001317022.1:p.Thr1355=
NM_001330094.1:c.4056G>A	NP_001317023.1:p.Thr1352=
NM_001330095.1:c.3927G>A	NP_001317024.1:p.Thr1309=
NM_001330096.1:c.3867G>A	NP_001317025.1:p.Thr1289=
NM_001330097.1:c.873G>A	NP_001317026.1:p.Thr291=
NM_004801.5:c.3978G>A	NP_004792.1:p.Thr1326=
NM_138735.4:c.873G>A	NP_620072.1:p.Thr291=
XM_005264642.4:c.4089G>A	XP_005264699.1:p.Thr1363=
XM_006712137.4:c.3999G>A	XP_006712200.1:p.Thr1333=
XM_006712140.4:c.4116G>A	XP_006712203.2:p.Thr1372=
XM_011533167.3:c.4089G>A	XP_011531469.1:p.Thr1363=
XM_011533172.3:c.4062G>A	XP_011531474.1:p.Thr1354=
XM_011533175.3:c.4032G>A	XP_011531477.1:p.Thr1344=
XM_011533177.3:c.3999G>A	XP_011531479.1:p.Thr1333=
XM_011533178.3:c.3999G>A	XP_011531480.1:p.Thr1333=
XM_011533180.3:c.4089G>A	XP_011531482.1:p.Thr1363=
XM_011533183.2:c.3222G>A	XP_011531485.1:p.Thr1074=
XM_017005303.2:c.4116G>A	XP_016860792.1:p.Thr1372=
XM_017005304.2:c.4113G>A	XP_016860793.1:p.Thr1371=
XM_017005305.2:c.4116G>A	XP_016860794.1:p.Thr1372=
XM_017005306.2:c.4104G>A	XP_016860795.1:p.Thr1368=
XM_017005307.2:c.4098G>A	XP_016860796.1:p.Thr1366=
XM_017005308.2:c.4095G>A	XP_016860797.1:p.Thr1365=
XM_017005309.2:c.4089G>A	XP_016860798.1:p.Thr1363=
XM_017005310.2:c.4086G>A	XP_016860799.1:p.Thr1362=
XM_017005311.2:c.4071G>A	XP_016860800.1:p.Thr1357=
XM_017005314.2:c.4056G>A	XP_016860803.1:p.Thr1352=
XM_017005315.2:c.4062G>A	XP_016860804.1:p.Thr1354=
XM_017005316.2:c.4053G>A	XP_016860805.1:p.Thr1351=
XM_017005318.2:c.4044G>A	XP_016860807.1:p.Thr1348=
XM_017005320.2:c.4041G>A	XP_016860809.1:p.Thr1347=
XM_017005321.2:c.4026G>A	XP_016860810.1:p.Thr1342=
XM_017005322.2:c.4026G>A	XP_016860811.1:p.Thr1342=
XM_017005324.2:c.3972G>A	XP_016860813.1:p.Thr1324=
XM_017005325.2:c.3972G>A	XP_016860814.1:p.Thr1324=
XM_017005326.2:c.3960G>A	XP_016860815.1:p.Thr1320=
XM_017005327.2:c.3954G>A	XP_016860816.1:p.Thr1318=
XM_017005329.2:c.4116G>A	XP_016860818.1:p.Thr1372=
XM_017005334.2:c.3156G>A	XP_016860823.1:p.Thr1052=
NM_001330078.2:c.4068G>A MANE Select	NP_001317007.1:p.Thr1356=
NM_001135659.3:c.4188G>A	NP_001129131.1:p.Thr1396=
NM_001330077.2:c.4044G>A	NP_001317006.1:p.Thr1348=
NM_001330082.2:c.4044G>A	NP_001317011.1:p.Thr1348=
NM_001330083.2:c.3912G>A	NP_001317012.1:p.Thr1304=
NM_001330084.2:c.4002G>A	NP_001317013.1:p.Thr1334=
NM_001330085.2:c.4041G>A	NP_001317014.1:p.Thr1347=
NM_001330086.2:c.4068G>A	NP_001317015.1:p.Thr1356=
NM_001330087.2:c.3867G>A	NP_001317016.1:p.Thr1289=
NM_001330088.2:c.3897G>A	NP_001317017.1:p.Thr1299=
NM_001330091.2:c.963G>A	NP_001317020.1:p.Thr321=
NM_001330092.2:c.963G>A	NP_001317021.1:p.Thr321=
NM_001330093.2:c.4065G>A	NP_001317022.1:p.Thr1355=
NM_001330094.2:c.4056G>A	NP_001317023.1:p.Thr1352=
NM_001330095.2:c.3927G>A	NP_001317024.1:p.Thr1309=
NM_001330096.2:c.3867G>A	NP_001317025.1:p.Thr1289=
NM_001330097.2:c.873G>A	NP_001317026.1:p.Thr291=
NM_004801.6:c.3978G>A	NP_004792.1:p.Thr1326=
NM_138735.5:c.873G>A	NP_620072.1:p.Thr291=