Canonical Allele Identifier: CA883006655

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1157785739
• MyVariant Identifiers: chr19:g.48923079_48923090del (hg19) ; chr19:g.48419822_48419833del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419827_48419838del , CM000681.2:g.48419827_48419838del	GRCh38
NC_000019.9:g.48923084_48923095del , CM000681.1:g.48923084_48923095del	GRCh37
NC_000019.8:g.53614896_53614907del	NCBI36
NG_052829.1:g.29953_29964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.2091+13_2091+24del MANE Select	ENSP00000263269.2:n.2091+13_2091+24del
ENST00000263269.3:c.2091+13_2091+24del	ENSP00000263269.2:n.2091+13_2091+24del
NM_000836.2:c.2091+13_2091+24del	NP_000827.2:n.2091+13_2091+24del
XM_011526872.1:c.2091+13_2091+24del	XP_011525174.1:n.2091+13_2091+24del
NM_000836.4:c.2091+13_2091+24del MANE Select	NP_000827.2:n.2091+13_2091+24del