Canonical Allele Identifier: CA2339887523
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419508_48419509delinsGT , CM000681.2:g.48419508_48419509delinsGT GRCh38
NC_000019.9:g.48922765_48922766delinsGT , CM000681.1:g.48922765_48922766delinsGT GRCh37
NC_000019.8:g.53614577_53614578delinsGT NCBI36
NG_052829.1:g.29634_29635delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-77_1862-76delinsGT MANE Select ENSP00000263269.2:n.1862-77_1862-76delinsGT
ENST00000263269.3:c.1862-77_1862-76delinsGT ENSP00000263269.2:n.1862-77_1862-76delinsGT
NM_000836.2:c.1862-77_1862-76delinsGT NP_000827.2:n.1862-77_1862-76delinsGT
XM_011526872.1:c.1862-77_1862-76delinsGT XP_011525174.1:n.1862-77_1862-76delinsGT
NM_000836.4:c.1862-77_1862-76delinsGT MANE Select NP_000827.2:n.1862-77_1862-76delinsGT