Canonical Allele Identifier: CA1515334709

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687581C= , CM000666.2:g.176687581C= GRCh38
NC_000004.11:g.177608735C= , CM000666.1:g.177608735C= GRCh37
NC_000004.10:g.177845729C= NCBI36
NG_034216.1:g.110165G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-61G= (VEGFC) MANE Select ENSP00000480043.1:n.812-61G=
ENST00000618562.1:c.812-61G= (VEGFC) ENSP00000480043.1:n.812-61G=
NM_005429.4:c.812-61G= (VEGFC) NP_005420.1:n.812-61G=
XR_939498.1:n.260+7831C= (HAFML)
XR_939499.1:n.209+17872C= (HAFML)
XR_939498.2:n.347+7831C= (HAFML)
XR_939499.2:n.292+17872C= (HAFML)
NM_005429.5:c.812-61G= (VEGFC) MANE Select NP_005420.1:n.812-61G=