Canonical Allele Identifier: CA356913029

Gene: KDR

Linked Data

• dbSNP Id: rs2110027441
• MyVariant Identifiers: chr4:g.55976666C>T (hg19) ; chr4:g.55110499C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55110499C>T , CM000666.2:g.55110499C>T	GRCh38
NC_000004.11:g.55976666C>T , CM000666.1:g.55976666C>T	GRCh37
NC_000004.10:g.55671423C>T	NCBI36
NG_012004.1:g.20097G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.1159G>A MANE Select	ENSP00000263923.4:p.Glu387Lys
ENST00000647068.1:n.1172G>A
ENST00000263923.4:c.1159G>A	ENSP00000263923.4:p.Glu387Lys
ENST00000512566.1:n.1159G>A
NM_002253.2:c.1159G>A	NP_002244.1:p.Glu387Lys
NM_002253.3:c.1159G>A	NP_002244.1:p.Glu387Lys
NM_002253.4:c.1159G>A MANE Select	NP_002244.1:p.Glu387Lys