Canonical Allele Identifier: CA356913474

Gene: KDR

Linked Data

• dbSNP Id: rs763780611
• MyVariant Identifiers: chr4:g.55976869A>T (hg19) ; chr4:g.55110702A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55110702A>T , CM000666.2:g.55110702A>T	GRCh38
NC_000004.11:g.55976869A>T , CM000666.1:g.55976869A>T	GRCh37
NC_000004.10:g.55671626A>T	NCBI36
NG_012004.1:g.19894T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.1043T>A MANE Select	ENSP00000263923.4:p.Val348Asp
ENST00000647068.1:n.1056T>A
ENST00000263923.4:c.1043T>A	ENSP00000263923.4:p.Val348Asp
ENST00000512566.1:n.1043T>A
NM_002253.2:c.1043T>A	NP_002244.1:p.Val348Asp
NM_002253.3:c.1043T>A	NP_002244.1:p.Val348Asp
NM_002253.4:c.1043T>A MANE Select	NP_002244.1:p.Val348Asp