Canonical Allele Identifier: CA1884328038

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137156719C= , CM000671.2:g.137156719C=	GRCh38
NC_000009.11:g.140051171C= , CM000671.1:g.140051171C=	GRCh37
NC_000009.10:g.139170992C=	NCBI36
NG_011507.1:g.22563C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.785C=	ENSP00000360608.3:p.Thr262=
ENST00000371560.5:c.785C=	ENSP00000360615.3:p.Thr262=
ENST00000371561.8:c.722C= MANE Select	ENSP00000360616.3:p.Thr241=
ENST00000675295.1:n.152C=
ENST00000676396.1:n.2232C=
ENST00000350902.9:c.785C=	ENSP00000316915.9:p.Thr262=
ENST00000371546.8:c.785C=	ENSP00000360601.4:p.Thr262=
ENST00000371550.8:c.722C=	ENSP00000360605.4:p.Thr241=
ENST00000371553.7:c.785C=	ENSP00000360608.3:p.Thr262=
ENST00000371555.8:c.785C=	ENSP00000360610.4:p.Thr262=
ENST00000371559.8:c.722C=	ENSP00000360614.4:p.Thr241=
ENST00000371560.4:c.785C=	ENSP00000360615.3:p.Thr262=
ENST00000371561.7:c.722C=	ENSP00000360616.3:p.Thr241=
ENST00000471122.5:n.799C=
NM_000832.6:c.722C=	NP_000823.4:p.Thr241=
NM_001185090.1:c.785C=	NP_001172019.1:p.Thr262=
NM_001185091.1:c.785C=	NP_001172020.1:p.Thr262=
NM_007327.3:c.722C=	NP_015566.1:p.Thr241=
NM_021569.3:c.722C=	NP_067544.1:p.Thr241=
XM_005266071.2:c.722C=	XP_005266128.1:p.Thr241=
XM_005266072.2:c.785C=	XP_005266129.1:p.Thr262=
XM_005266073.3:c.785C=	XP_005266130.1:p.Thr262=
XM_011518583.1:c.785C=	XP_011516885.1:p.Thr262=
XM_005266071.3:c.722C=	XP_005266128.1:p.Thr241=
XM_005266072.3:c.785C=	XP_005266129.1:p.Thr262=
XM_005266073.4:c.785C=	XP_005266130.1:p.Thr262=
XM_011518583.2:c.785C=	XP_011516885.1:p.Thr262=
NM_007327.4:c.722C= MANE Select	NP_015566.1:p.Thr241=
NM_000832.7:c.722C=	NP_000823.4:p.Thr241=
NM_001185090.2:c.785C=	NP_001172019.1:p.Thr262=
NM_001185091.2:c.785C=	NP_001172020.1:p.Thr262=
NM_021569.4:c.722C=	NP_067544.1:p.Thr241=