Canonical Allele Identifier: CA358824540

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687465C>G , CM000666.2:g.176687465C>G GRCh38
NC_000004.11:g.177608619C>G , CM000666.1:g.177608619C>G GRCh37
NC_000004.10:g.177845613C>G NCBI36
NG_034216.1:g.110281G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.867G>C (VEGFC) MANE Select ENSP00000480043.1:p.Glu289Asp
ENST00000618562.1:c.867G>C (VEGFC) ENSP00000480043.1:p.Glu289Asp
NM_005429.4:c.867G>C (VEGFC) NP_005420.1:p.Glu289Asp
XR_939498.1:n.260+7715C>G (HAFML)
XR_939499.1:n.209+17756C>G (HAFML)
XR_939498.2:n.347+7715C>G (HAFML)
XR_939499.2:n.292+17756C>G (HAFML)
NM_005429.5:c.867G>C (VEGFC) MANE Select NP_005420.1:p.Glu289Asp