Canonical Allele Identifier: CA2339887527

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1970990266
• gnomAD v4: 19-48419509-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419511_48419512del , CM000681.2:g.48419511_48419512del	GRCh38
NC_000019.9:g.48922768_48922769del , CM000681.1:g.48922768_48922769del	GRCh37
NC_000019.8:g.53614580_53614581del	NCBI36
NG_052829.1:g.29637_29638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-74_1862-73del MANE Select	ENSP00000263269.2:n.1862-74_1862-73del
ENST00000263269.3:c.1862-74_1862-73del	ENSP00000263269.2:n.1862-74_1862-73del
NM_000836.2:c.1862-74_1862-73del	NP_000827.2:n.1862-74_1862-73del
XM_011526872.1:c.1862-74_1862-73del	XP_011525174.1:n.1862-74_1862-73del
NM_000836.4:c.1862-74_1862-73del MANE Select	NP_000827.2:n.1862-74_1862-73del