Canonical Allele Identifier: CA2770853721

Gene: VEGFA POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43785368C>A , CM000668.2:g.43785368C>A	GRCh38
NC_000006.11:g.43753105C>A , CM000668.1:g.43753105C>A	GRCh37
NC_000006.10:g.43861083C>A	NCBI36
NG_008732.1:g.20153C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425836.9:c.*740C>A (VEGFA)	ENSP00000388465.4:n.*740C>A
ENST00000425836.8:c.*740C>A (VEGFA)	ENSP00000388465.4:n.*740C>A
ENST00000672860.3:c.*806C>A (VEGFA) MANE Select	ENSP00000500082.3:n.*806C>A
ENST00000372064.9:c.1790C>A (VEGFA)	ENSP00000361134.5:n.1790C>A
ENST00000372067.8:c.*806C>A (VEGFA)	ENSP00000361137.4:n.*806C>A
ENST00000672860.2:c.*740C>A (VEGFA)	ENSP00000500082.2:n.*740C>A
ENST00000372064.8:c.1790C>A (VEGFA)	ENSP00000361134.4:n.1790C>A
ENST00000372067.7:c.*806C>A (VEGFA)	ENSP00000361137.3:n.*806C>A
ENST00000372077.8:c.*806C>A (VEGFA)	ENSP00000361148.4:n.*806C>A
ENST00000480614.1:n.11051C>A (VEGFA)
ENST00000497139.5:n.1675C>A (VEGFA)
ENST00000611736.4:c.*806C>A (VEGFA)	ENSP00000478570.1:n.*806C>A
ENST00000615393.4:c.*806C>A (VEGFA)	ENSP00000478034.1:n.*806C>A
ENST00000617771.4:c.*806C>A (VEGFA)	ENSP00000484284.1:n.*806C>A
ENST00000621747.4:c.*806C>A (VEGFA)	ENSP00000483241.1:n.*806C>A
NM_001025366.2:c.*806C>A (VEGFA)	NP_001020537.2:n.*806C>A
NM_001025367.2:c.*806C>A (VEGFA)	NP_001020538.2:n.*806C>A
NM_001025368.2:c.*806C>A (VEGFA)	NP_001020539.2:n.*806C>A
NM_001025369.2:c.*822C>A (VEGFA)	NP_001020540.2:n.*822C>A
NM_001025370.2:c.*806C>A (VEGFA)	NP_001020541.2:n.*806C>A
NM_001033756.2:c.*740C>A (VEGFA)	NP_001028928.1:n.*740C>A
NM_001171622.1:c.*806C>A (VEGFA)	NP_001165093.1:n.*806C>A
NM_001171623.1:c.*806C>A (VEGFA)	NP_001165094.1:n.*806C>A
NM_001171624.1:c.*806C>A (VEGFA)	NP_001165095.1:n.*806C>A
NM_001171625.1:c.*806C>A (VEGFA)	NP_001165096.1:n.*806C>A
NM_001171626.1:c.*806C>A (VEGFA)	NP_001165097.1:n.*806C>A
NM_001171627.1:c.*822C>A (VEGFA)	NP_001165098.1:n.*822C>A
NM_001171628.1:c.*806C>A (VEGFA)	NP_001165099.1:n.*806C>A
NM_001171629.1:c.*740C>A (VEGFA)	NP_001165100.1:n.*740C>A
NM_001171630.1:c.*806C>A (VEGFA)	NP_001165101.1:n.*806C>A
NM_001204384.1:c.*806C>A (VEGFA)	NP_001191313.1:n.*806C>A
NM_001204385.1:c.*806C>A (VEGFA)	NP_001191314.1:n.*806C>A
NM_001287044.1:c.*806C>A (VEGFA)	NP_001273973.1:n.*806C>A
NM_001317010.1:c.*740C>A (VEGFA)	NP_001303939.1:n.*740C>A
NM_003376.5:c.*806C>A (VEGFA)	NP_003367.4:n.*806C>A
NM_001025366.3:c.*806C>A (VEGFA)	NP_001020537.2:n.*806C>A
NM_001025367.3:c.*806C>A (VEGFA)	NP_001020538.2:n.*806C>A
NM_001025368.3:c.*806C>A (VEGFA)	NP_001020539.2:n.*806C>A
NM_001025369.3:c.*822C>A (VEGFA)	NP_001020540.2:n.*822C>A
NM_001025370.3:c.*806C>A (VEGFA)	NP_001020541.2:n.*806C>A
NM_001033756.3:c.*740C>A (VEGFA)	NP_001028928.1:n.*740C>A
NM_001171622.2:c.*806C>A (VEGFA)	NP_001165093.1:n.*806C>A
NM_001204385.2:c.*806C>A (VEGFA)	NP_001191314.1:n.*806C>A
NM_001287044.2:c.*806C>A (VEGFA)	NP_001273973.1:n.*806C>A
NM_003376.6:c.*806C>A (VEGFA) MANE Select	NP_003367.4:n.*806C>A
NM_001171623.2:c.*806C>A (VEGFA)	NP_001165094.1:n.*806C>A
NM_001171624.2:c.*806C>A (VEGFA)	NP_001165095.1:n.*806C>A
NM_001171625.2:c.*806C>A (VEGFA)	NP_001165096.1:n.*806C>A
NM_001171626.2:c.*806C>A (VEGFA)	NP_001165097.1:n.*806C>A
NM_001171627.2:c.*822C>A (VEGFA)	NP_001165098.1:n.*822C>A
NM_001171628.2:c.*806C>A (VEGFA)	NP_001165099.1:n.*806C>A
NM_001171629.2:c.*740C>A (VEGFA)	NP_001165100.1:n.*740C>A
NM_001171630.2:c.*806C>A (VEGFA)	NP_001165101.1:n.*806C>A
NM_001204384.2:c.*806C>A (VEGFA)	NP_001191313.1:n.*806C>A
NM_001318876.2:c.945+256097C>A (POLR1C)	NP_001305805.1:n.945+256097C>A