Canonical Allele Identifier: CA2509223229

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419516_48419517insC , CM000681.2:g.48419516_48419517insC	GRCh38
NC_000019.9:g.48922773_48922774insC , CM000681.1:g.48922773_48922774insC	GRCh37
NC_000019.8:g.53614585_53614586insC	NCBI36
NG_052829.1:g.29642_29643insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-69_1862-68insC MANE Select	ENSP00000263269.2:n.1862-69_1862-68insC
ENST00000263269.3:c.1862-69_1862-68insC	ENSP00000263269.2:n.1862-69_1862-68insC
NM_000836.2:c.1862-69_1862-68insC	NP_000827.2:n.1862-69_1862-68insC
XM_011526872.1:c.1862-69_1862-68insC	XP_011525174.1:n.1862-69_1862-68insC
NM_000836.4:c.1862-69_1862-68insC MANE Select	NP_000827.2:n.1862-69_1862-68insC