Canonical Allele Identifier: CA375729574

Gene: GRIN1

Linked Data

• dbSNP Id: rs1833941322
• gnomAD v4: 9-137167423-G-A
• MyVariant Identifiers: chr9:g.140061875G>A (hg19) ; chr9:g.137167423G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167423G>A , CM000671.2:g.137167423G>A	GRCh38
NC_000009.11:g.140061875G>A , CM000671.1:g.140061875G>A	GRCh37
NC_000009.10:g.139181696G>A	NCBI36
NG_011507.1:g.33267G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-351G>A	ENSP00000360608.3:n.2764-351G>A
ENST00000371560.5:c.2653-351G>A	ENSP00000360615.3:n.2653-351G>A
ENST00000371561.8:c.2713G>A MANE Select	ENSP00000360616.3:p.Gly905Arg
ENST00000371546.8:c.2776G>A	ENSP00000360601.4:p.Gly926Arg
ENST00000371550.8:c.2602G>A	ENSP00000360605.4:p.Gly868Arg
ENST00000371553.7:c.2764-351G>A	ENSP00000360608.3:n.2764-351G>A
ENST00000371555.8:c.2665G>A	ENSP00000360610.4:p.Gly889Arg
ENST00000371559.8:c.2590-351G>A	ENSP00000360614.4:n.2590-351G>A
ENST00000371560.4:c.2653-351G>A	ENSP00000360615.3:n.2653-351G>A
ENST00000371561.7:c.2713G>A	ENSP00000360616.3:p.Gly905Arg
ENST00000473811.1:n.193G>A
NM_000832.6:c.2590-351G>A	NP_000823.4:n.2590-351G>A
NM_001185090.1:c.2764-351G>A	NP_001172019.1:n.2764-351G>A
NM_001185091.1:c.2653-351G>A	NP_001172020.1:n.2653-351G>A
NM_007327.3:c.2713G>A	NP_015566.1:p.Gly905Arg
NM_021569.3:c.2602G>A	NP_067544.1:p.Gly868Arg
XM_005266071.2:c.2701-351G>A	XP_005266128.1:n.2701-351G>A
XM_005266072.2:c.2665G>A	XP_005266129.1:p.Gly889Arg
XM_005266073.3:c.2776G>A	XP_005266130.1:p.Gly926Arg
XM_005266071.3:c.2701-351G>A	XP_005266128.1:n.2701-351G>A
XM_005266072.3:c.2665G>A	XP_005266129.1:p.Gly889Arg
XM_005266073.4:c.2776G>A	XP_005266130.1:p.Gly926Arg
NM_007327.4:c.2713G>A MANE Select	NP_015566.1:p.Gly905Arg
NM_000832.7:c.2590-351G>A	NP_000823.4:n.2590-351G>A
NM_001185090.2:c.2764-351G>A	NP_001172019.1:n.2764-351G>A
NM_001185091.2:c.2653-351G>A	NP_001172020.1:n.2653-351G>A
NM_021569.4:c.2602G>A	NP_067544.1:p.Gly868Arg