Canonical Allele Identifier: CA1458928367
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091695A= , CM000666.2:g.55091695A= GRCh38
NC_000004.11:g.55957862A= , CM000666.1:g.55957862A= GRCh37
NC_000004.10:g.55652619A= NCBI36
NG_012004.1:g.38901T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+922T= MANE Select ENSP00000263923.4:n.3069+922T=
ENST00000647068.1:n.3082+922T=
ENST00000263923.4:c.3069+922T= ENSP00000263923.4:n.3069+922T=
NM_002253.2:c.3069+922T= NP_002244.1:n.3069+922T=
NM_002253.3:c.3069+922T= NP_002244.1:n.3069+922T=
NM_002253.4:c.3069+922T= MANE Select NP_002244.1:n.3069+922T=