Canonical Allele Identifier: CA2339887536

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1970990893

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419518_48419519insC , CM000681.2:g.48419518_48419519insC	GRCh38
NC_000019.9:g.48922775_48922776insC , CM000681.1:g.48922775_48922776insC	GRCh37
NC_000019.8:g.53614587_53614588insC	NCBI36
NG_052829.1:g.29644_29645insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-67_1862-66insC MANE Select	ENSP00000263269.2:n.1862-67_1862-66insC
ENST00000263269.3:c.1862-67_1862-66insC	ENSP00000263269.2:n.1862-67_1862-66insC
NM_000836.2:c.1862-67_1862-66insC	NP_000827.2:n.1862-67_1862-66insC
XM_011526872.1:c.1862-67_1862-66insC	XP_011525174.1:n.1862-67_1862-66insC
NM_000836.4:c.1862-67_1862-66insC MANE Select	NP_000827.2:n.1862-67_1862-66insC