Canonical Allele Identifier: CA2586189609
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419567del , CM000681.2:g.48419567del GRCh38
NC_000019.9:g.48922824del , CM000681.1:g.48922824del GRCh37
NC_000019.8:g.53614636del NCBI36
NG_052829.1:g.29693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-18del MANE Select ENSP00000263269.2:n.1862-18del
ENST00000263269.3:c.1862-18del ENSP00000263269.2:n.1862-18del
NM_000836.2:c.1862-18del NP_000827.2:n.1862-18del
XM_011526872.1:c.1862-18del XP_011525174.1:n.1862-18del
NM_000836.4:c.1862-18del MANE Select NP_000827.2:n.1862-18del