Canonical Allele Identifier: CA2586189599

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419555-GGTCCATGTCCACGTCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419557_48419573del , CM000681.2:g.48419557_48419573del	GRCh38
NC_000019.9:g.48922814_48922830del , CM000681.1:g.48922814_48922830del	GRCh37
NC_000019.8:g.53614626_53614642del	NCBI36
NG_052829.1:g.29683_29699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-28_1862-12del MANE Select	ENSP00000263269.2:n.1862-28_1862-12del
ENST00000263269.3:c.1862-28_1862-12del	ENSP00000263269.2:n.1862-28_1862-12del
NM_000836.2:c.1862-28_1862-12del	NP_000827.2:n.1862-28_1862-12del
XM_011526872.1:c.1862-28_1862-12del	XP_011525174.1:n.1862-28_1862-12del
NM_000836.4:c.1862-28_1862-12del MANE Select	NP_000827.2:n.1862-28_1862-12del