Canonical Allele Identifier: CA356921485
Gene: KDR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125266C>G , CM000666.2:g.55125266C>G GRCh38
NC_000004.11:g.55991433C>G , CM000666.1:g.55991433C>G GRCh37
NC_000004.10:g.55686190C>G NCBI36
NG_012004.1:g.5330G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.28G>C MANE Select ENSP00000263923.4:p.Ala10Pro
ENST00000263923.4:c.28G>C ENSP00000263923.4:p.Ala10Pro
ENST00000512566.1:n.28G>C
NM_002253.2:c.28G>C NP_002244.1:p.Ala10Pro
NM_002253.3:c.28G>C NP_002244.1:p.Ala10Pro
NM_002253.4:c.28G>C MANE Select NP_002244.1:p.Ala10Pro