Canonical Allele Identifier: CA356913443

Gene: KDR

Linked Data

• dbSNP Id: rs2110027979
• COSMIC: COSM4912564
• MyVariant Identifiers: chr4:g.55976858C>A (hg19) ; chr4:g.55110691C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55110691C>A , CM000666.2:g.55110691C>A	GRCh38
NC_000004.11:g.55976858C>A , CM000666.1:g.55976858C>A	GRCh37
NC_000004.10:g.55671615C>A	NCBI36
NG_012004.1:g.19905G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.1054G>T MANE Select	ENSP00000263923.4:p.Ala352Ser
ENST00000647068.1:n.1067G>T
ENST00000263923.4:c.1054G>T	ENSP00000263923.4:p.Ala352Ser
ENST00000512566.1:n.1054G>T
NM_002253.2:c.1054G>T	NP_002244.1:p.Ala352Ser
NM_002253.3:c.1054G>T	NP_002244.1:p.Ala352Ser
NM_002253.4:c.1054G>T MANE Select	NP_002244.1:p.Ala352Ser