Canonical Allele Identifier: CA1458940169
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125319C= , CM000666.2:g.55125319C= GRCh38
NC_000004.11:g.55991486C= , CM000666.1:g.55991486C= GRCh37
NC_000004.10:g.55686243C= NCBI36
NG_012004.1:g.5277G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-26G= MANE Select ENSP00000263923.4:n.-26G=
ENST00000263923.4:c.-26G= ENSP00000263923.4:n.-26G=
NM_002253.2:c.-26G= NP_002244.1:n.-26G=
NM_002253.3:c.-26G= NP_002244.1:n.-26G=
NM_002253.4:c.-26G= MANE Select NP_002244.1:n.-26G=