Canonical Allele Identifier: CA2339887543
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419528_48419529delinsTC , CM000681.2:g.48419528_48419529delinsTC GRCh38
NC_000019.9:g.48922785_48922786delinsTC , CM000681.1:g.48922785_48922786delinsTC GRCh37
NC_000019.8:g.53614597_53614598delinsTC NCBI36
NG_052829.1:g.29654_29655delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-57_1862-56delinsTC MANE Select ENSP00000263269.2:n.1862-57_1862-56delinsTC
ENST00000263269.3:c.1862-57_1862-56delinsTC ENSP00000263269.2:n.1862-57_1862-56delinsTC
NM_000836.2:c.1862-57_1862-56delinsTC NP_000827.2:n.1862-57_1862-56delinsTC
XM_011526872.1:c.1862-57_1862-56delinsTC XP_011525174.1:n.1862-57_1862-56delinsTC
NM_000836.4:c.1862-57_1862-56delinsTC MANE Select NP_000827.2:n.1862-57_1862-56delinsTC