Canonical Allele Identifier: CA2692773902

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137139196-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137139196G>T , CM000671.2:g.137139196G>T	GRCh38
NC_000009.11:g.140033648G>T , CM000671.1:g.140033648G>T	GRCh37
NC_000009.10:g.139153469G>T	NCBI36
NG_011507.1:g.5040G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.-291G>T	ENSP00000360608.3:n.-291G>T
ENST00000371560.5:c.-291G>T	ENSP00000360615.3:n.-291G>T
ENST00000371561.8:c.-291G>T MANE Select	ENSP00000360616.3:n.-291G>T
ENST00000350902.9:c.-291G>T	ENSP00000316915.9:n.-291G>T
ENST00000371561.7:c.-291G>T	ENSP00000360616.3:n.-291G>T
NM_000832.6:c.-291G>T	NP_000823.4:n.-291G>T
NM_001185090.1:c.-291G>T	NP_001172019.1:n.-291G>T
NM_001185091.1:c.-291G>T	NP_001172020.1:n.-291G>T
NM_007327.3:c.-291G>T	NP_015566.1:n.-291G>T
NM_021569.3:c.-291G>T	NP_067544.1:n.-291G>T
XM_005266071.2:c.-291G>T	XP_005266128.1:n.-291G>T
XM_005266072.2:c.-291G>T	XP_005266129.1:n.-291G>T
XM_005266073.3:c.-291G>T	XP_005266130.1:n.-291G>T
XM_011518583.1:c.-291G>T	XP_011516885.1:n.-291G>T
XM_005266072.3:c.-291G>T	XP_005266129.1:n.-291G>T
XM_005266073.4:c.-291G>T	XP_005266130.1:n.-291G>T
XM_011518583.2:c.-291G>T	XP_011516885.1:n.-291G>T
NM_007327.4:c.-291G>T MANE Select	NP_015566.1:n.-291G>T
NM_000832.7:c.-291G>T	NP_000823.4:n.-291G>T
NM_001185090.2:c.-291G>T	NP_001172019.1:n.-291G>T
NM_001185091.2:c.-291G>T	NP_001172020.1:n.-291G>T
NM_021569.4:c.-291G>T	NP_067544.1:n.-291G>T