Canonical Allele Identifier: CA358824534

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687463G>T , CM000666.2:g.176687463G>T GRCh38
NC_000004.11:g.177608617G>T , CM000666.1:g.177608617G>T GRCh37
NC_000004.10:g.177845611G>T NCBI36
NG_034216.1:g.110283C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.869C>A (VEGFC) MANE Select ENSP00000480043.1:p.Thr290Asn
ENST00000618562.1:c.869C>A (VEGFC) ENSP00000480043.1:p.Thr290Asn
NM_005429.4:c.869C>A (VEGFC) NP_005420.1:p.Thr290Asn
XR_939498.1:n.260+7713G>T (HAFML)
XR_939499.1:n.209+17754G>T (HAFML)
XR_939498.2:n.347+7713G>T (HAFML)
XR_939499.2:n.292+17754G>T (HAFML)
NM_005429.5:c.869C>A (VEGFC) MANE Select NP_005420.1:p.Thr290Asn