Canonical Allele Identifier: CA2339887584
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419628G= , CM000681.2:g.48419628G= GRCh38
NC_000019.9:g.48922885G= , CM000681.1:g.48922885G= GRCh37
NC_000019.8:g.53614697G= NCBI36
NG_052829.1:g.29754G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1905G= MANE Select ENSP00000263269.2:p.Leu635=
ENST00000263269.3:c.1905G= ENSP00000263269.2:p.Leu635=
NM_000836.2:c.1905G= NP_000827.2:p.Leu635=
XM_011526872.1:c.1905G= XP_011525174.1:p.Leu635=
NM_000836.4:c.1905G= MANE Select NP_000827.2:p.Leu635=