Canonical Allele Identifier: CA2339887544

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419529_48419533delinsCCCTT , CM000681.2:g.48419529_48419533delinsCCCTT	GRCh38
NC_000019.9:g.48922786_48922790delinsCCCTT , CM000681.1:g.48922786_48922790delinsCCCTT	GRCh37
NC_000019.8:g.53614598_53614602delinsCCCTT	NCBI36
NG_052829.1:g.29655_29659delinsCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-56_1862-52delinsCCCTT MANE Select	ENSP00000263269.2:n.1862-56_1862-52delinsCCCTT
ENST00000263269.3:c.1862-56_1862-52delinsCCCTT	ENSP00000263269.2:n.1862-56_1862-52delinsCCCTT
NM_000836.2:c.1862-56_1862-52delinsCCCTT	NP_000827.2:n.1862-56_1862-52delinsCCCTT
XM_011526872.1:c.1862-56_1862-52delinsCCCTT	XP_011525174.1:n.1862-56_1862-52delinsCCCTT
NM_000836.4:c.1862-56_1862-52delinsCCCTT MANE Select	NP_000827.2:n.1862-56_1862-52delinsCCCTT