Canonical Allele Identifier: CA556933062

Linked Data

dbSNP Id: rs1219599145

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687563_176687569del , CM000666.2:g.176687563_176687569del GRCh38
NC_000004.11:g.177608717_177608723del , CM000666.1:g.177608717_177608723del GRCh37
NC_000004.10:g.177845711_177845717del NCBI36
NG_034216.1:g.110180_110186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-46_812-40del (VEGFC) MANE Select ENSP00000480043.1:n.812-46_812-40del
ENST00000618562.1:c.812-46_812-40del (VEGFC) ENSP00000480043.1:n.812-46_812-40del
NM_005429.4:c.812-46_812-40del (VEGFC) NP_005420.1:n.812-46_812-40del
XR_939498.1:n.260+7813_260+7819del (HAFML)
XR_939499.1:n.209+17854_209+17860del (HAFML)
XR_939498.2:n.347+7813_347+7819del (HAFML)
XR_939499.2:n.292+17854_292+17860del (HAFML)
NM_005429.5:c.812-46_812-40del (VEGFC) MANE Select NP_005420.1:n.812-46_812-40del