Canonical Allele Identifier: CA2586189546

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419514-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419515del , CM000681.2:g.48419515del	GRCh38
NC_000019.9:g.48922772del , CM000681.1:g.48922772del	GRCh37
NC_000019.8:g.53614584del	NCBI36
NG_052829.1:g.29641del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-70del MANE Select	ENSP00000263269.2:n.1862-70del
ENST00000263269.3:c.1862-70del	ENSP00000263269.2:n.1862-70del
NM_000836.2:c.1862-70del	NP_000827.2:n.1862-70del
XM_011526872.1:c.1862-70del	XP_011525174.1:n.1862-70del
NM_000836.4:c.1862-70del MANE Select	NP_000827.2:n.1862-70del