Canonical Allele Identifier: CA920124701

Gene: GRIN2D

Linked Data

• dbSNP Id: rs11302654
• gnomAD v4: 19-48419515-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419527_48419528dup , CM000681.2:g.48419527_48419528dup	GRCh38
NC_000019.9:g.48922784_48922785dup , CM000681.1:g.48922784_48922785dup	GRCh37
NC_000019.8:g.53614596_53614597dup	NCBI36
NG_052829.1:g.29653_29654dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-58_1862-57dup MANE Select	ENSP00000263269.2:n.1862-58_1862-57dup
ENST00000263269.3:c.1862-58_1862-57dup	ENSP00000263269.2:n.1862-58_1862-57dup
NM_000836.2:c.1862-58_1862-57dup	NP_000827.2:n.1862-58_1862-57dup
XM_011526872.1:c.1862-58_1862-57dup	XP_011525174.1:n.1862-58_1862-57dup
NM_000836.4:c.1862-58_1862-57dup MANE Select	NP_000827.2:n.1862-58_1862-57dup