Canonical Allele Identifier: CA2339887524

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419508_48419512delinsGTTCT , CM000681.2:g.48419508_48419512delinsGTTCT	GRCh38
NC_000019.9:g.48922765_48922769delinsGTTCT , CM000681.1:g.48922765_48922769delinsGTTCT	GRCh37
NC_000019.8:g.53614577_53614581delinsGTTCT	NCBI36
NG_052829.1:g.29634_29638delinsGTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-77_1862-73delinsGTTCT MANE Select	ENSP00000263269.2:n.1862-77_1862-73delinsGTTCT
ENST00000263269.3:c.1862-77_1862-73delinsGTTCT	ENSP00000263269.2:n.1862-77_1862-73delinsGTTCT
NM_000836.2:c.1862-77_1862-73delinsGTTCT	NP_000827.2:n.1862-77_1862-73delinsGTTCT
XM_011526872.1:c.1862-77_1862-73delinsGTTCT	XP_011525174.1:n.1862-77_1862-73delinsGTTCT
NM_000836.4:c.1862-77_1862-73delinsGTTCT MANE Select	NP_000827.2:n.1862-77_1862-73delinsGTTCT