Canonical Allele Identifier: CA2692778948

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137167358-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167361del , CM000671.2:g.137167361del	GRCh38
NC_000009.11:g.140061813del , CM000671.1:g.140061813del	GRCh37
NC_000009.10:g.139181634del	NCBI36
NG_011507.1:g.33205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2764-413del	ENSP00000360608.3:n.2764-413del
ENST00000371560.5:c.2653-413del	ENSP00000360615.3:n.2653-413del
ENST00000371561.8:c.2701-50del MANE Select	ENSP00000360616.3:n.2701-50del
ENST00000371546.8:c.2764-50del	ENSP00000360601.4:n.2764-50del
ENST00000371550.8:c.2590-50del	ENSP00000360605.4:n.2590-50del
ENST00000371553.7:c.2764-413del	ENSP00000360608.3:n.2764-413del
ENST00000371555.8:c.2653-50del	ENSP00000360610.4:n.2653-50del
ENST00000371559.8:c.2590-413del	ENSP00000360614.4:n.2590-413del
ENST00000371560.4:c.2653-413del	ENSP00000360615.3:n.2653-413del
ENST00000371561.7:c.2701-50del	ENSP00000360616.3:n.2701-50del
ENST00000473811.1:n.181-50del
NM_000832.6:c.2590-413del	NP_000823.4:n.2590-413del
NM_001185090.1:c.2764-413del	NP_001172019.1:n.2764-413del
NM_001185091.1:c.2653-413del	NP_001172020.1:n.2653-413del
NM_007327.3:c.2701-50del	NP_015566.1:n.2701-50del
NM_021569.3:c.2590-50del	NP_067544.1:n.2590-50del
XM_005266071.2:c.2701-413del	XP_005266128.1:n.2701-413del
XM_005266072.2:c.2653-50del	XP_005266129.1:n.2653-50del
XM_005266073.3:c.2764-50del	XP_005266130.1:n.2764-50del
XM_005266071.3:c.2701-413del	XP_005266128.1:n.2701-413del
XM_005266072.3:c.2653-50del	XP_005266129.1:n.2653-50del
XM_005266073.4:c.2764-50del	XP_005266130.1:n.2764-50del
NM_007327.4:c.2701-50del MANE Select	NP_015566.1:n.2701-50del
NM_000832.7:c.2590-413del	NP_000823.4:n.2590-413del
NM_001185090.2:c.2764-413del	NP_001172019.1:n.2764-413del
NM_001185091.2:c.2653-413del	NP_001172020.1:n.2653-413del
NM_021569.4:c.2590-50del	NP_067544.1:n.2590-50del