Canonical Allele Identifier: CA1515334704

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687559T= , CM000666.2:g.176687559T= GRCh38
NC_000004.11:g.177608713T= , CM000666.1:g.177608713T= GRCh37
NC_000004.10:g.177845707T= NCBI36
NG_034216.1:g.110187A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-39A= (VEGFC) MANE Select ENSP00000480043.1:n.812-39A=
ENST00000618562.1:c.812-39A= (VEGFC) ENSP00000480043.1:n.812-39A=
NM_005429.4:c.812-39A= (VEGFC) NP_005420.1:n.812-39A=
XR_939498.1:n.260+7809T= (HAFML)
XR_939499.1:n.209+17850T= (HAFML)
XR_939498.2:n.347+7809T= (HAFML)
XR_939499.2:n.292+17850T= (HAFML)
NM_005429.5:c.812-39A= (VEGFC) MANE Select NP_005420.1:n.812-39A=