Canonical Allele Identifier: CA1458932521
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110604G= , CM000666.2:g.55110604G= GRCh38
NC_000004.11:g.55976771G= , CM000666.1:g.55976771G= GRCh37
NC_000004.10:g.55671528G= NCBI36
NG_012004.1:g.19992C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1092-38C= MANE Select ENSP00000263923.4:n.1092-38C=
ENST00000647068.1:n.1105-38C=
ENST00000263923.4:c.1092-38C= ENSP00000263923.4:n.1092-38C=
ENST00000512566.1:n.1092-38C=
NM_002253.2:c.1092-38C= NP_002244.1:n.1092-38C=
NM_002253.3:c.1092-38C= NP_002244.1:n.1092-38C=
NM_002253.4:c.1092-38C= MANE Select NP_002244.1:n.1092-38C=