Canonical Allele Identifier: CA2586189506

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419485-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419486_48419487dup , CM000681.2:g.48419486_48419487dup	GRCh38
NC_000019.9:g.48922743_48922744dup , CM000681.1:g.48922743_48922744dup	GRCh37
NC_000019.8:g.53614555_53614556dup	NCBI36
NG_052829.1:g.29612_29613dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-99_1862-98dup MANE Select	ENSP00000263269.2:n.1862-99_1862-98dup
ENST00000263269.3:c.1862-99_1862-98dup	ENSP00000263269.2:n.1862-99_1862-98dup
NM_000836.2:c.1862-99_1862-98dup	NP_000827.2:n.1862-99_1862-98dup
XM_011526872.1:c.1862-99_1862-98dup	XP_011525174.1:n.1862-99_1862-98dup
NM_000836.4:c.1862-99_1862-98dup MANE Select	NP_000827.2:n.1862-99_1862-98dup