Canonical Allele Identifier: CA5361074

Gene: GRIN1

Linked Data

• dbSNP Id: rs778757411
• ExAC: 9:140057593 G / A
• gnomAD v2: 9-140057593-G-A
• gnomAD v3: 9-137163141-G-A
• gnomAD v4: 9-137163141-G-A
• MyVariant Identifiers: chr9:g.140057593G>A (hg19) ; chr9:g.140057593_140057594delinsAC (hg19) ; chr9:g.137163141G>A (hg38) ; chr9:g.137163141_137163142delinsAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137163141G>A , CM000671.2:g.137163141G>A	GRCh38
NC_000009.11:g.140057593G>A , CM000671.1:g.140057593G>A	GRCh37
NC_000009.10:g.139177414G>A	NCBI36
NG_011507.1:g.28985G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2235-28G>A	ENSP00000360608.3:n.2235-28G>A
ENST00000371560.5:c.2235-28G>A	ENSP00000360615.3:n.2235-28G>A
ENST00000371561.8:c.2172-28G>A MANE Select	ENSP00000360616.3:n.2172-28G>A
ENST00000675295.1:n.1602-28G>A
ENST00000350902.9:c.*1147-28G>A	ENSP00000316915.9:n.*1147-28G>A
ENST00000371546.8:c.2235-28G>A	ENSP00000360601.4:n.2235-28G>A
ENST00000371550.8:c.2172-28G>A	ENSP00000360605.4:n.2172-28G>A
ENST00000371553.7:c.2235-28G>A	ENSP00000360608.3:n.2235-28G>A
ENST00000371555.8:c.2235-28G>A	ENSP00000360610.4:n.2235-28G>A
ENST00000371559.8:c.2172-28G>A	ENSP00000360614.4:n.2172-28G>A
ENST00000371560.4:c.2235-28G>A	ENSP00000360615.3:n.2235-28G>A
ENST00000371561.7:c.2172-28G>A	ENSP00000360616.3:n.2172-28G>A
ENST00000460273.1:n.193-28G>A
ENST00000471122.5:n.2249-28G>A
NM_000832.6:c.2172-28G>A	NP_000823.4:n.2172-28G>A
NM_001185090.1:c.2235-28G>A	NP_001172019.1:n.2235-28G>A
NM_001185091.1:c.2235-28G>A	NP_001172020.1:n.2235-28G>A
NM_007327.3:c.2172-28G>A	NP_015566.1:n.2172-28G>A
NM_021569.3:c.2172-28G>A	NP_067544.1:n.2172-28G>A
XM_005266071.2:c.2172-28G>A	XP_005266128.1:n.2172-28G>A
XM_005266072.2:c.2235-28G>A	XP_005266129.1:n.2235-28G>A
XM_005266073.3:c.2235-28G>A	XP_005266130.1:n.2235-28G>A
XM_011518583.1:c.2235-28G>A	XP_011516885.1:n.2235-28G>A
XM_005266071.3:c.2172-28G>A	XP_005266128.1:n.2172-28G>A
XM_005266072.3:c.2235-28G>A	XP_005266129.1:n.2235-28G>A
XM_005266073.4:c.2235-28G>A	XP_005266130.1:n.2235-28G>A
XM_011518583.2:c.2235-28G>A	XP_011516885.1:n.2235-28G>A
NM_007327.4:c.2172-28G>A MANE Select	NP_015566.1:n.2172-28G>A
NM_000832.7:c.2172-28G>A	NP_000823.4:n.2172-28G>A
NM_001185090.2:c.2235-28G>A	NP_001172019.1:n.2235-28G>A
NM_001185091.2:c.2235-28G>A	NP_001172020.1:n.2235-28G>A
NM_021569.4:c.2172-28G>A	NP_067544.1:n.2172-28G>A