Canonical Allele Identifier: CA2692779303

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137167444-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167449del , CM000671.2:g.137167449del	GRCh38
NC_000009.11:g.140061901del , CM000671.1:g.140061901del	GRCh37
NC_000009.10:g.139181722del	NCBI36
NG_011507.1:g.33293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2764-325del	ENSP00000360608.3:n.2764-325del
ENST00000371560.5:c.2653-325del	ENSP00000360615.3:n.2653-325del
ENST00000371561.8:c.2739del MANE Select	ENSP00000360616.3:p.Asp914ThrfsTer?
ENST00000371546.8:c.2802del	ENSP00000360601.4:p.Asp935ThrfsTer?
ENST00000371550.8:c.2628del	ENSP00000360605.4:p.Asp877ThrfsTer?
ENST00000371553.7:c.2764-325del	ENSP00000360608.3:n.2764-325del
ENST00000371555.8:c.2691del	ENSP00000360610.4:p.Asp898ThrfsTer?
ENST00000371559.8:c.2590-325del	ENSP00000360614.4:n.2590-325del
ENST00000371560.4:c.2653-325del	ENSP00000360615.3:n.2653-325del
ENST00000371561.7:c.2739del	ENSP00000360616.3:p.Asp914ThrfsTer?
ENST00000473811.1:n.219del
NM_000832.6:c.2590-325del	NP_000823.4:n.2590-325del
NM_001185090.1:c.2764-325del	NP_001172019.1:n.2764-325del
NM_001185091.1:c.2653-325del	NP_001172020.1:n.2653-325del
NM_007327.3:c.2739del	NP_015566.1:p.Asp914ThrfsTer?
NM_021569.3:c.2628del	NP_067544.1:p.Asp877ThrfsTer?
XM_005266071.2:c.2701-325del	XP_005266128.1:n.2701-325del
XM_005266072.2:c.2691del	XP_005266129.1:p.Asp898ThrfsTer?
XM_005266073.3:c.2802del	XP_005266130.1:p.Asp935ThrfsTer?
XM_005266071.3:c.2701-325del	XP_005266128.1:n.2701-325del
XM_005266072.3:c.2691del	XP_005266129.1:p.Asp898ThrfsTer?
XM_005266073.4:c.2802del	XP_005266130.1:p.Asp935ThrfsTer?
NM_007327.4:c.2739del MANE Select	NP_015566.1:p.Asp914ThrfsTer?
NM_000832.7:c.2590-325del	NP_000823.4:n.2590-325del
NM_001185090.2:c.2764-325del	NP_001172019.1:n.2764-325del
NM_001185091.2:c.2653-325del	NP_001172020.1:n.2653-325del
NM_021569.4:c.2628del	NP_067544.1:p.Asp877ThrfsTer?