Canonical Allele Identifier: CA2339887551
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419540_48419545delinsTGAGAA , CM000681.2:g.48419540_48419545delinsTGAGAA GRCh38
NC_000019.9:g.48922797_48922802delinsTGAGAA , CM000681.1:g.48922797_48922802delinsTGAGAA GRCh37
NC_000019.8:g.53614609_53614614delinsTGAGAA NCBI36
NG_052829.1:g.29666_29671delinsTGAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-45_1862-40delinsTGAGAA MANE Select ENSP00000263269.2:n.1862-45_1862-40delinsTGAGAA
ENST00000263269.3:c.1862-45_1862-40delinsTGAGAA ENSP00000263269.2:n.1862-45_1862-40delinsTGAGAA
NM_000836.2:c.1862-45_1862-40delinsTGAGAA NP_000827.2:n.1862-45_1862-40delinsTGAGAA
XM_011526872.1:c.1862-45_1862-40delinsTGAGAA XP_011525174.1:n.1862-45_1862-40delinsTGAGAA
NM_000836.4:c.1862-45_1862-40delinsTGAGAA MANE Select NP_000827.2:n.1862-45_1862-40delinsTGAGAA