Canonical Allele Identifier: CA2586189556

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419527-TTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419528_48419530del , CM000681.2:g.48419528_48419530del	GRCh38
NC_000019.9:g.48922785_48922787del , CM000681.1:g.48922785_48922787del	GRCh37
NC_000019.8:g.53614597_53614599del	NCBI36
NG_052829.1:g.29654_29656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-57_1862-55del MANE Select	ENSP00000263269.2:n.1862-57_1862-55del
ENST00000263269.3:c.1862-57_1862-55del	ENSP00000263269.2:n.1862-57_1862-55del
NM_000836.2:c.1862-57_1862-55del	NP_000827.2:n.1862-57_1862-55del
XM_011526872.1:c.1862-57_1862-55del	XP_011525174.1:n.1862-57_1862-55del
NM_000836.4:c.1862-57_1862-55del MANE Select	NP_000827.2:n.1862-57_1862-55del