Canonical Allele Identifier: CA1884333330

Gene: GRIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167445A= , CM000671.2:g.137167445A=	GRCh38
NC_000009.11:g.140061897A= , CM000671.1:g.140061897A=	GRCh37
NC_000009.10:g.139181718A=	NCBI36
NG_011507.1:g.33289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2764-329A=	ENSP00000360608.3:n.2764-329A=
ENST00000371560.5:c.2653-329A=	ENSP00000360615.3:n.2653-329A=
ENST00000371561.8:c.2735A= MANE Select	ENSP00000360616.3:p.Gln912=
ENST00000371546.8:c.2798A=	ENSP00000360601.4:p.Gln933=
ENST00000371550.8:c.2624A=	ENSP00000360605.4:p.Gln875=
ENST00000371553.7:c.2764-329A=	ENSP00000360608.3:n.2764-329A=
ENST00000371555.8:c.2687A=	ENSP00000360610.4:p.Gln896=
ENST00000371559.8:c.2590-329A=	ENSP00000360614.4:n.2590-329A=
ENST00000371560.4:c.2653-329A=	ENSP00000360615.3:n.2653-329A=
ENST00000371561.7:c.2735A=	ENSP00000360616.3:p.Gln912=
ENST00000473811.1:n.215A=
NM_000832.6:c.2590-329A=	NP_000823.4:n.2590-329A=
NM_001185090.1:c.2764-329A=	NP_001172019.1:n.2764-329A=
NM_001185091.1:c.2653-329A=	NP_001172020.1:n.2653-329A=
NM_007327.3:c.2735A=	NP_015566.1:p.Gln912=
NM_021569.3:c.2624A=	NP_067544.1:p.Gln875=
XM_005266071.2:c.2701-329A=	XP_005266128.1:n.2701-329A=
XM_005266072.2:c.2687A=	XP_005266129.1:p.Gln896=
XM_005266073.3:c.2798A=	XP_005266130.1:p.Gln933=
XM_005266071.3:c.2701-329A=	XP_005266128.1:n.2701-329A=
XM_005266072.3:c.2687A=	XP_005266129.1:p.Gln896=
XM_005266073.4:c.2798A=	XP_005266130.1:p.Gln933=
NM_007327.4:c.2735A= MANE Select	NP_015566.1:p.Gln912=
NM_000832.7:c.2590-329A=	NP_000823.4:n.2590-329A=
NM_001185090.2:c.2764-329A=	NP_001172019.1:n.2764-329A=
NM_001185091.2:c.2653-329A=	NP_001172020.1:n.2653-329A=
NM_021569.4:c.2624A=	NP_067544.1:p.Gln875=