Canonical Allele Identifier: CA1458940049
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125074A= , CM000666.2:g.55125074A= GRCh38
NC_000004.11:g.55991241A= , CM000666.1:g.55991241A= GRCh37
NC_000004.10:g.55685998A= NCBI36
NG_012004.1:g.5522T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+153T= MANE Select ENSP00000263923.4:n.67+153T=
ENST00000263923.4:c.67+153T= ENSP00000263923.4:n.67+153T=
ENST00000512566.1:n.67+153T=
NM_002253.2:c.67+153T= NP_002244.1:n.67+153T=
NM_002253.3:c.67+153T= NP_002244.1:n.67+153T=
NM_002253.4:c.67+153T= MANE Select NP_002244.1:n.67+153T=