Canonical Allele Identifier: CA111350156

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176689730T>A , CM000666.2:g.176689730T>A GRCh38
NC_000004.11:g.177610884T>A , CM000666.1:g.177610884T>A GRCh37
NC_000004.10:g.177847878T>A NCBI36
NG_034216.1:g.108016A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.705-1803A>T (VEGFC) MANE Select ENSP00000480043.1:n.705-1803A>T
ENST00000507638.1:n.404-75A>T (VEGFC)
ENST00000618562.1:c.705-1803A>T (VEGFC) ENSP00000480043.1:n.705-1803A>T
NM_005429.4:c.705-1803A>T (VEGFC) NP_005420.1:n.705-1803A>T
XR_939498.1:n.260+9980T>A (HAFML)
XR_939499.1:n.210-16173T>A (HAFML)
XR_939498.2:n.347+9980T>A (HAFML)
XR_939499.2:n.293-16173T>A (HAFML)
NM_005429.5:c.705-1803A>T (VEGFC) MANE Select NP_005420.1:n.705-1803A>T