Canonical Allele Identifier: CA2586189501
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419483_48419495del , CM000681.2:g.48419483_48419495del GRCh38
NC_000019.9:g.48922740_48922752del , CM000681.1:g.48922740_48922752del GRCh37
NC_000019.8:g.53614552_53614564del NCBI36
NG_052829.1:g.29609_29621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-102_1862-90del MANE Select ENSP00000263269.2:n.1862-102_1862-90del
ENST00000263269.3:c.1862-102_1862-90del ENSP00000263269.2:n.1862-102_1862-90del
NM_000836.2:c.1862-102_1862-90del NP_000827.2:n.1862-102_1862-90del
XM_011526872.1:c.1862-102_1862-90del XP_011525174.1:n.1862-102_1862-90del
NM_000836.4:c.1862-102_1862-90del MANE Select NP_000827.2:n.1862-102_1862-90del