Canonical Allele Identifier: CA358824544

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687467C>A , CM000666.2:g.176687467C>A GRCh38
NC_000004.11:g.177608621C>A , CM000666.1:g.177608621C>A GRCh37
NC_000004.10:g.177845615C>A NCBI36
NG_034216.1:g.110279G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.865G>T (VEGFC) MANE Select ENSP00000480043.1:p.Glu289Ter
ENST00000618562.1:c.865G>T (VEGFC) ENSP00000480043.1:p.Glu289Ter
NM_005429.4:c.865G>T (VEGFC) NP_005420.1:p.Glu289Ter
XR_939498.1:n.260+7717C>A (HAFML)
XR_939499.1:n.209+17758C>A (HAFML)
XR_939498.2:n.347+7717C>A (HAFML)
XR_939499.2:n.292+17758C>A (HAFML)
NM_005429.5:c.865G>T (VEGFC) MANE Select NP_005420.1:p.Glu289Ter