Canonical Allele Identifier: CA883006257

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1343798947
• gnomAD v4: 19-48419511-CTTTCT-C
• MyVariant Identifiers: chr19:g.48922769_48922773del (hg19) ; chr19:g.48419512_48419516del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419515_48419519del , CM000681.2:g.48419515_48419519del	GRCh38
NC_000019.9:g.48922772_48922776del , CM000681.1:g.48922772_48922776del	GRCh37
NC_000019.8:g.53614584_53614588del	NCBI36
NG_052829.1:g.29641_29645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-70_1862-66del MANE Select	ENSP00000263269.2:n.1862-70_1862-66del
ENST00000263269.3:c.1862-70_1862-66del	ENSP00000263269.2:n.1862-70_1862-66del
NM_000836.2:c.1862-70_1862-66del	NP_000827.2:n.1862-70_1862-66del
XM_011526872.1:c.1862-70_1862-66del	XP_011525174.1:n.1862-70_1862-66del
NM_000836.4:c.1862-70_1862-66del MANE Select	NP_000827.2:n.1862-70_1862-66del