Canonical Allele Identifier: CA2586189559

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419528-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419530_48419531dup , CM000681.2:g.48419530_48419531dup	GRCh38
NC_000019.9:g.48922787_48922788dup , CM000681.1:g.48922787_48922788dup	GRCh37
NC_000019.8:g.53614599_53614600dup	NCBI36
NG_052829.1:g.29656_29657dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-55_1862-54dup MANE Select	ENSP00000263269.2:n.1862-55_1862-54dup
ENST00000263269.3:c.1862-55_1862-54dup	ENSP00000263269.2:n.1862-55_1862-54dup
NM_000836.2:c.1862-55_1862-54dup	NP_000827.2:n.1862-55_1862-54dup
XM_011526872.1:c.1862-55_1862-54dup	XP_011525174.1:n.1862-55_1862-54dup
NM_000836.4:c.1862-55_1862-54dup MANE Select	NP_000827.2:n.1862-55_1862-54dup