Canonical Allele Identifier: CA406698457

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48923069A>T (hg19) ; chr19:g.48419812A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419812A>T , CM000681.2:g.48419812A>T	GRCh38
NC_000019.9:g.48923069A>T , CM000681.1:g.48923069A>T	GRCh37
NC_000019.8:g.53614881A>T	NCBI36
NG_052829.1:g.29938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.2089A>T MANE Select	ENSP00000263269.2:p.Lys697Ter
ENST00000263269.3:c.2089A>T	ENSP00000263269.2:p.Lys697Ter
NM_000836.2:c.2089A>T	NP_000827.2:p.Lys697Ter
XM_011526872.1:c.2089A>T	XP_011525174.1:p.Lys697Ter
NM_000836.4:c.2089A>T MANE Select	NP_000827.2:p.Lys697Ter