Canonical Allele Identifier: CA2339887563
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419574_48419575delinsGC , CM000681.2:g.48419574_48419575delinsGC GRCh38
NC_000019.9:g.48922831_48922832delinsGC , CM000681.1:g.48922831_48922832delinsGC GRCh37
NC_000019.8:g.53614643_53614644delinsGC NCBI36
NG_052829.1:g.29700_29701delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-11_1862-10delinsGC MANE Select ENSP00000263269.2:n.1862-11_1862-10delinsGC
ENST00000263269.3:c.1862-11_1862-10delinsGC ENSP00000263269.2:n.1862-11_1862-10delinsGC
NM_000836.2:c.1862-11_1862-10delinsGC NP_000827.2:n.1862-11_1862-10delinsGC
XM_011526872.1:c.1862-11_1862-10delinsGC XP_011525174.1:n.1862-11_1862-10delinsGC
NM_000836.4:c.1862-11_1862-10delinsGC MANE Select NP_000827.2:n.1862-11_1862-10delinsGC