Canonical Allele Identifier: CA996593875

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1970996686
• gnomAD v3: 19-48419829-AGGGCTGGGCTGGAGCTG-A
• gnomAD v4: 19-48419829-AGGGCTGGGCTGGAGCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419838_48419854del , CM000681.2:g.48419838_48419854del	GRCh38
NC_000019.9:g.48923095_48923111del , CM000681.1:g.48923095_48923111del	GRCh37
NC_000019.8:g.53614907_53614923del	NCBI36
NG_052829.1:g.29964_29980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.2091+24_2091+40del MANE Select	ENSP00000263269.2:n.2091+24_2091+40del
ENST00000263269.3:c.2091+24_2091+40del	ENSP00000263269.2:n.2091+24_2091+40del
NM_000836.2:c.2091+24_2091+40del	NP_000827.2:n.2091+24_2091+40del
XM_011526872.1:c.2091+24_2091+40del	XP_011525174.1:n.2091+24_2091+40del
NM_000836.4:c.2091+24_2091+40del MANE Select	NP_000827.2:n.2091+24_2091+40del