Canonical Allele Identifier: CA1458933526
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112719G= , CM000666.2:g.55112719G= GRCh38
NC_000004.11:g.55978886G= , CM000666.1:g.55978886G= GRCh37
NC_000004.10:g.55673643G= NCBI36
NG_012004.1:g.17877C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+585C= MANE Select ENSP00000263923.4:n.976+585C=
ENST00000647068.1:n.989+585C=
ENST00000263923.4:c.976+585C= ENSP00000263923.4:n.976+585C=
ENST00000512566.1:n.976+585C=
NM_002253.2:c.976+585C= NP_002244.1:n.976+585C=
NM_002253.3:c.976+585C= NP_002244.1:n.976+585C=
NM_002253.4:c.976+585C= MANE Select NP_002244.1:n.976+585C=