Canonical Allele Identifier: CA1884333278

Gene: GRIN1

Linked Data

• dbSNP Id: rs1833934717
• gnomAD v4: 9-137167326-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167326G>A , CM000671.2:g.137167326G>A	GRCh38
NC_000009.11:g.140061778G>A , CM000671.1:g.140061778G>A	GRCh37
NC_000009.10:g.139181599G>A	NCBI36
NG_011507.1:g.33170G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-448G>A	ENSP00000360608.3:n.2764-448G>A
ENST00000371560.5:c.2653-448G>A	ENSP00000360615.3:n.2653-448G>A
ENST00000371561.8:c.2701-85G>A MANE Select	ENSP00000360616.3:n.2701-85G>A
ENST00000371546.8:c.2764-85G>A	ENSP00000360601.4:n.2764-85G>A
ENST00000371550.8:c.2590-85G>A	ENSP00000360605.4:n.2590-85G>A
ENST00000371553.7:c.2764-448G>A	ENSP00000360608.3:n.2764-448G>A
ENST00000371555.8:c.2653-85G>A	ENSP00000360610.4:n.2653-85G>A
ENST00000371559.8:c.2590-448G>A	ENSP00000360614.4:n.2590-448G>A
ENST00000371560.4:c.2653-448G>A	ENSP00000360615.3:n.2653-448G>A
ENST00000371561.7:c.2701-85G>A	ENSP00000360616.3:n.2701-85G>A
ENST00000473811.1:n.181-85G>A
NM_000832.6:c.2590-448G>A	NP_000823.4:n.2590-448G>A
NM_001185090.1:c.2764-448G>A	NP_001172019.1:n.2764-448G>A
NM_001185091.1:c.2653-448G>A	NP_001172020.1:n.2653-448G>A
NM_007327.3:c.2701-85G>A	NP_015566.1:n.2701-85G>A
NM_021569.3:c.2590-85G>A	NP_067544.1:n.2590-85G>A
XM_005266071.2:c.2701-448G>A	XP_005266128.1:n.2701-448G>A
XM_005266072.2:c.2653-85G>A	XP_005266129.1:n.2653-85G>A
XM_005266073.3:c.2764-85G>A	XP_005266130.1:n.2764-85G>A
XM_005266071.3:c.2701-448G>A	XP_005266128.1:n.2701-448G>A
XM_005266072.3:c.2653-85G>A	XP_005266129.1:n.2653-85G>A
XM_005266073.4:c.2764-85G>A	XP_005266130.1:n.2764-85G>A
NM_007327.4:c.2701-85G>A MANE Select	NP_015566.1:n.2701-85G>A
NM_000832.7:c.2590-448G>A	NP_000823.4:n.2590-448G>A
NM_001185090.2:c.2764-448G>A	NP_001172019.1:n.2764-448G>A
NM_001185091.2:c.2653-448G>A	NP_001172020.1:n.2653-448G>A
NM_021569.4:c.2590-85G>A	NP_067544.1:n.2590-85G>A