Canonical Allele Identifier: CA1458940123
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125238G= , CM000666.2:g.55125238G= GRCh38
NC_000004.11:g.55991405G= , CM000666.1:g.55991405G= GRCh37
NC_000004.10:g.55686162G= NCBI36
NG_012004.1:g.5358C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.56C= MANE Select ENSP00000263923.4:p.Ala19=
ENST00000263923.4:c.56C= ENSP00000263923.4:p.Ala19=
ENST00000512566.1:n.56C=
NM_002253.2:c.56C= NP_002244.1:p.Ala19=
NM_002253.3:c.56C= NP_002244.1:p.Ala19=
NM_002253.4:c.56C= MANE Select NP_002244.1:p.Ala19=