Canonical Allele Identifier: CA5360574

Gene: GRIN1

Linked Data

• dbSNP Id: rs770981821
• ExAC: 9:140033996 G / A
• gnomAD v2: 9-140033996-G-A
• gnomAD v4: 9-137139544-G-A
• MyVariant Identifiers: chr9:g.140033996G>A (hg19) ; chr9:g.137139544G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139544G>A , CM000671.2:g.137139544G>A	GRCh38
NC_000009.11:g.140033996G>A , CM000671.1:g.140033996G>A	GRCh37
NC_000009.10:g.139153817G>A	NCBI36
NG_011507.1:g.5388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.58G>A	ENSP00000360608.3:p.Ala20Thr
ENST00000371560.5:c.58G>A	ENSP00000360615.3:p.Ala20Thr
ENST00000371561.8:c.58G>A MANE Select	ENSP00000360616.3:p.Ala20Thr
ENST00000350902.9:c.58G>A	ENSP00000316915.9:p.Ala20Thr
ENST00000371546.8:c.58G>A	ENSP00000360601.4:p.Ala20Thr
ENST00000371550.8:c.58G>A	ENSP00000360605.4:p.Ala20Thr
ENST00000371553.7:c.58G>A	ENSP00000360608.3:p.Ala20Thr
ENST00000371555.8:c.58G>A	ENSP00000360610.4:p.Ala20Thr
ENST00000371559.8:c.58G>A	ENSP00000360614.4:p.Ala20Thr
ENST00000371560.4:c.58G>A	ENSP00000360615.3:p.Ala20Thr
ENST00000371561.7:c.58G>A	ENSP00000360616.3:p.Ala20Thr
ENST00000471122.5:n.135G>A
NM_000832.6:c.58G>A	NP_000823.4:p.Ala20Thr
NM_001185090.1:c.58G>A	NP_001172019.1:p.Ala20Thr
NM_001185091.1:c.58G>A	NP_001172020.1:p.Ala20Thr
NM_007327.3:c.58G>A	NP_015566.1:p.Ala20Thr
NM_021569.3:c.58G>A	NP_067544.1:p.Ala20Thr
XM_005266071.2:c.58G>A	XP_005266128.1:p.Ala20Thr
XM_005266072.2:c.58G>A	XP_005266129.1:p.Ala20Thr
XM_005266073.3:c.58G>A	XP_005266130.1:p.Ala20Thr
XM_011518583.1:c.58G>A	XP_011516885.1:p.Ala20Thr
XM_005266071.3:c.58G>A	XP_005266128.1:p.Ala20Thr
XM_005266072.3:c.58G>A	XP_005266129.1:p.Ala20Thr
XM_005266073.4:c.58G>A	XP_005266130.1:p.Ala20Thr
XM_011518583.2:c.58G>A	XP_011516885.1:p.Ala20Thr
NM_007327.4:c.58G>A MANE Select	NP_015566.1:p.Ala20Thr
NM_000832.7:c.58G>A	NP_000823.4:p.Ala20Thr
NM_001185090.2:c.58G>A	NP_001172019.1:p.Ala20Thr
NM_001185091.2:c.58G>A	NP_001172020.1:p.Ala20Thr
NM_021569.4:c.58G>A	NP_067544.1:p.Ala20Thr