Canonical Allele Identifier: CA6871078

Gene: UBC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124913493G>C , CM000674.2:g.124913493G>C	GRCh38
NC_000012.11:g.125398039G>C , CM000674.1:g.125398039G>C	GRCh37
NC_000012.10:g.123963992G>C	NCBI36
NG_027722.2:g.6549C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339647.6:c.279C>G MANE Select	ENSP00000344818.5:p.Val93=
ENST00000339647.5:c.279C>G	ENSP00000344818.5:p.Val93=
ENST00000535131.1:c.279C>G	ENSP00000439492.1:p.Val93=
ENST00000535859.1:c.279C>G	ENSP00000437452.1:p.Val93=
ENST00000536769.1:c.279C>G	ENSP00000441543.1:p.Val93=
ENST00000538617.5:c.279C>G	ENSP00000443053.1:p.Val93=
ENST00000540351.1:c.279C>G	ENSP00000442800.1:p.Val93=
ENST00000540700.1:c.279C>G	ENSP00000441238.1:p.Val93=
ENST00000541272.1:c.276+3C>G	ENSP00000440205.1:n.276+3C>G
ENST00000541645.1:c.279C>G	ENSP00000445337.1:p.Val93=
ENST00000544481.1:n.334C>G
ENST00000546120.2:c.279C>G	ENSP00000438394.2:p.Val93=
ENST00000546271.1:c.279C>G	ENSP00000438289.1:p.Val93=
NM_021009.6:c.279C>G	NP_066289.3:p.Val93=
NM_021009.7:c.279C>G MANE Select	NP_066289.3:p.Val93=