Canonical Allele Identifier: CA382944370

Gene: HYOU1

Linked Data

• MyVariant Identifiers: chr11:g.119052773G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119052773G>T , CM000673.2:g.119052773G>T	GRCh38
NC_000011.8:g.118428695G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527038.7:c.851C>A	ENSP00000463742.3:p.Ala284Asp
ENST00000530467.6:c.851C>A	ENSP00000479845.2:p.Ala284Asp
ENST00000530473.6:c.851C>A	ENSP00000431874.2:p.Ala284Asp
ENST00000532421.6:c.851C>A	ENSP00000463515.2:p.Ala284Asp
ENST00000532519.7:c.851C>A	ENSP00000467866.3:p.Ala284Asp
ENST00000533381.6:n.1088C>A
ENST00000534233.6:c.851C>A	ENSP00000462951.2:p.Ala284Asp
ENST00000610597.2:c.851C>A	ENSP00000484622.2:p.Ala284Asp
ENST00000614711.5:c.851C>A	ENSP00000480248.2:p.Ala284Asp
ENST00000694929.1:n.1405C>A
ENST00000694930.1:n.1041C>A
ENST00000694932.1:c.851C>A	ENSP00000511598.1:p.Ala284Asp
ENST00000694933.1:c.851C>A	ENSP00000511599.1:p.Ala284Asp
ENST00000694934.1:c.851C>A	ENSP00000511600.1:p.Ala284Asp
ENST00000694935.1:c.851C>A	ENSP00000511601.1:p.Ala284Asp
ENST00000694937.1:c.*370C>A	ENSP00000511603.1:n.*370C>A
ENST00000617285.5:c.851C>A MANE Select	ENSP00000480150.1:p.Ala284Asp
ENST00000652093.1:c.851C>A	ENSP00000498353.1:p.Ala284Asp
ENST00000530473.5:c.851C>A	ENSP00000431874.1:p.Ala284Asp
ENST00000531694.5:n.1957C>A
ENST00000532519.6:c.851C>A	ENSP00000467866.2:p.Ala284Asp
ENST00000543287.5:c.*640C>A	ENSP00000442727.2:n.*640C>A
ENST00000612687.4:c.851C>A	ENSP00000483106.1:p.Ala284Asp
ENST00000614668.4:c.436+2271C>A	ENSP00000482199.1:n.436+2271C>A
ENST00000614711.4:c.851C>A	ENSP00000480248.1:p.Ala284Asp
ENST00000617285.4:c.851C>A	ENSP00000480150.1:p.Ala284Asp
ENST00000621959.4:c.851C>A	ENSP00000484186.1:p.Ala284Asp
NM_001130991.2:c.851C>A	NP_001124463.1:p.Ala284Asp
NM_006389.4:c.851C>A	NP_006380.1:p.Ala284Asp
XM_005271392.2:c.851C>A	XP_005271449.1:p.Ala284Asp
XM_005271393.2:c.851C>A	XP_005271450.1:p.Ala284Asp
XM_005271394.2:c.851C>A	XP_005271451.1:p.Ala284Asp
XM_011542557.1:c.983C>A	XP_011540859.1:p.Ala328Asp
XM_011542558.1:c.983C>A	XP_011540860.1:p.Ala328Asp
XR_947790.1:n.998C>A
XM_005271392.4:c.851C>A	XP_005271449.1:p.Ala284Asp
XM_005271393.3:c.851C>A	XP_005271450.1:p.Ala284Asp
XM_005271394.3:c.851C>A	XP_005271451.1:p.Ala284Asp
XM_017017095.1:c.851C>A	XP_016872584.1:p.Ala284Asp
XM_017017096.1:c.851C>A	XP_016872585.1:p.Ala284Asp
XM_017017097.1:c.851C>A	XP_016872586.1:p.Ala284Asp
XR_001747729.1:n.981C>A
XR_002957117.1:n.981C>A
NM_006389.5:c.851C>A MANE Select	NP_006380.1:p.Ala284Asp
NM_001130991.3:c.851C>A	NP_001124463.1:p.Ala284Asp