Canonical Allele Identifier: CA1884333247

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167258C= , CM000671.2:g.137167258C=	GRCh38
NC_000009.11:g.140061710C= , CM000671.1:g.140061710C=	GRCh37
NC_000009.10:g.139181531C=	NCBI36
NG_011507.1:g.33102C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-516C=	ENSP00000360608.3:n.2764-516C=
ENST00000371560.5:c.2653-516C=	ENSP00000360615.3:n.2653-516C=
ENST00000371561.8:c.2701-153C= MANE Select	ENSP00000360616.3:n.2701-153C=
ENST00000371546.8:c.2764-153C=	ENSP00000360601.4:n.2764-153C=
ENST00000371550.8:c.2590-153C=	ENSP00000360605.4:n.2590-153C=
ENST00000371553.7:c.2764-516C=	ENSP00000360608.3:n.2764-516C=
ENST00000371555.8:c.2653-153C=	ENSP00000360610.4:n.2653-153C=
ENST00000371559.8:c.2590-516C=	ENSP00000360614.4:n.2590-516C=
ENST00000371560.4:c.2653-516C=	ENSP00000360615.3:n.2653-516C=
ENST00000371561.7:c.2701-153C=	ENSP00000360616.3:n.2701-153C=
ENST00000473811.1:n.181-153C=
NM_000832.6:c.2590-516C=	NP_000823.4:n.2590-516C=
NM_001185090.1:c.2764-516C=	NP_001172019.1:n.2764-516C=
NM_001185091.1:c.2653-516C=	NP_001172020.1:n.2653-516C=
NM_007327.3:c.2701-153C=	NP_015566.1:n.2701-153C=
NM_021569.3:c.2590-153C=	NP_067544.1:n.2590-153C=
XM_005266071.2:c.2701-516C=	XP_005266128.1:n.2701-516C=
XM_005266072.2:c.2653-153C=	XP_005266129.1:n.2653-153C=
XM_005266073.3:c.2764-153C=	XP_005266130.1:n.2764-153C=
XM_005266071.3:c.2701-516C=	XP_005266128.1:n.2701-516C=
XM_005266072.3:c.2653-153C=	XP_005266129.1:n.2653-153C=
XM_005266073.4:c.2764-153C=	XP_005266130.1:n.2764-153C=
NM_007327.4:c.2701-153C= MANE Select	NP_015566.1:n.2701-153C=
NM_000832.7:c.2590-516C=	NP_000823.4:n.2590-516C=
NM_001185090.2:c.2764-516C=	NP_001172019.1:n.2764-516C=
NM_001185091.2:c.2653-516C=	NP_001172020.1:n.2653-516C=
NM_021569.4:c.2590-153C=	NP_067544.1:n.2590-153C=