Canonical Allele Identifier: CA2339887528

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419511_48419516delinsCTTTCT , CM000681.2:g.48419511_48419516delinsCTTTCT	GRCh38
NC_000019.9:g.48922768_48922773delinsCTTTCT , CM000681.1:g.48922768_48922773delinsCTTTCT	GRCh37
NC_000019.8:g.53614580_53614585delinsCTTTCT	NCBI36
NG_052829.1:g.29637_29642delinsCTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-74_1862-69delinsCTTTCT MANE Select	ENSP00000263269.2:n.1862-74_1862-69delinsCTTTCT
ENST00000263269.3:c.1862-74_1862-69delinsCTTTCT	ENSP00000263269.2:n.1862-74_1862-69delinsCTTTCT
NM_000836.2:c.1862-74_1862-69delinsCTTTCT	NP_000827.2:n.1862-74_1862-69delinsCTTTCT
XM_011526872.1:c.1862-74_1862-69delinsCTTTCT	XP_011525174.1:n.1862-74_1862-69delinsCTTTCT
NM_000836.4:c.1862-74_1862-69delinsCTTTCT MANE Select	NP_000827.2:n.1862-74_1862-69delinsCTTTCT