Canonical Allele Identifier: CA358824537

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687464T>C , CM000666.2:g.176687464T>C GRCh38
NC_000004.11:g.177608618T>C , CM000666.1:g.177608618T>C GRCh37
NC_000004.10:g.177845612T>C NCBI36
NG_034216.1:g.110282A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.868A>G (VEGFC) MANE Select ENSP00000480043.1:p.Thr290Ala
ENST00000618562.1:c.868A>G (VEGFC) ENSP00000480043.1:p.Thr290Ala
NM_005429.4:c.868A>G (VEGFC) NP_005420.1:p.Thr290Ala
XR_939498.1:n.260+7714T>C (HAFML)
XR_939499.1:n.209+17755T>C (HAFML)
XR_939498.2:n.347+7714T>C (HAFML)
XR_939499.2:n.292+17755T>C (HAFML)
NM_005429.5:c.868A>G (VEGFC) MANE Select NP_005420.1:p.Thr290Ala