Canonical Allele Identifier: CA375730173

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140061972A>C (hg19) ; chr9:g.137167520A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167520A>C , CM000671.2:g.137167520A>C	GRCh38
NC_000009.11:g.140061972A>C , CM000671.1:g.140061972A>C	GRCh37
NC_000009.10:g.139181793A>C	NCBI36
NG_011507.1:g.33364A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-254A>C	ENSP00000360608.3:n.2764-254A>C
ENST00000371560.5:c.2653-254A>C	ENSP00000360615.3:n.2653-254A>C
ENST00000371561.8:c.2810A>C MANE Select	ENSP00000360616.3:p.Glu937Ala
ENST00000371546.8:c.2873A>C	ENSP00000360601.4:p.Glu958Ala
ENST00000371550.8:c.2699A>C	ENSP00000360605.4:p.Glu900Ala
ENST00000371553.7:c.2764-254A>C	ENSP00000360608.3:n.2764-254A>C
ENST00000371555.8:c.2762A>C	ENSP00000360610.4:p.Glu921Ala
ENST00000371559.8:c.2590-254A>C	ENSP00000360614.4:n.2590-254A>C
ENST00000371560.4:c.2653-254A>C	ENSP00000360615.3:n.2653-254A>C
ENST00000371561.7:c.2810A>C	ENSP00000360616.3:p.Glu937Ala
ENST00000473811.1:n.290A>C
NM_000832.6:c.2590-254A>C	NP_000823.4:n.2590-254A>C
NM_001185090.1:c.2764-254A>C	NP_001172019.1:n.2764-254A>C
NM_001185091.1:c.2653-254A>C	NP_001172020.1:n.2653-254A>C
NM_007327.3:c.2810A>C	NP_015566.1:p.Glu937Ala
NM_021569.3:c.2699A>C	NP_067544.1:p.Glu900Ala
XM_005266071.2:c.2701-254A>C	XP_005266128.1:n.2701-254A>C
XM_005266072.2:c.2762A>C	XP_005266129.1:p.Glu921Ala
XM_005266073.3:c.2873A>C	XP_005266130.1:p.Glu958Ala
XM_005266071.3:c.2701-254A>C	XP_005266128.1:n.2701-254A>C
XM_005266072.3:c.2762A>C	XP_005266129.1:p.Glu921Ala
XM_005266073.4:c.2873A>C	XP_005266130.1:p.Glu958Ala
NM_007327.4:c.2810A>C MANE Select	NP_015566.1:p.Glu937Ala
NM_000832.7:c.2590-254A>C	NP_000823.4:n.2590-254A>C
NM_001185090.2:c.2764-254A>C	NP_001172019.1:n.2764-254A>C
NM_001185091.2:c.2653-254A>C	NP_001172020.1:n.2653-254A>C
NM_021569.4:c.2699A>C	NP_067544.1:p.Glu900Ala