Canonical Allele Identifier: CA1577025564
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478884C= , CM000667.2:g.119478884C= GRCh38
NC_000005.9:g.118814579C= , CM000667.1:g.118814579C= GRCh37
NC_000005.8:g.118842478C= NCBI36
NG_008182.1:g.31432C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.485C= ENSP00000426272.2:p.Ala162=
ENST00000518349.6:c.113-17659C= ENSP00000507185.1:n.113-17659C=
ENST00000682445.1:c.*366C= ENSP00000508061.1:n.*366C=
ENST00000682531.1:n.586C=
ENST00000682626.1:c.513C= ENSP00000507857.1:p.Gly171=
ENST00000682996.1:c.485C= ENSP00000507792.1:p.Ala162=
ENST00000683265.1:n.578C=
ENST00000683371.1:c.*615C= ENSP00000508376.1:n.*615C=
ENST00000683390.1:n.2175C=
ENST00000683549.1:n.406C=
ENST00000683936.1:c.*370C= ENSP00000507721.1:n.*370C=
ENST00000683974.1:n.567C=
ENST00000683996.1:c.74C= ENSP00000507060.1:p.Ala25=
ENST00000684131.1:n.324C=
ENST00000684160.1:c.*175C= ENSP00000507821.1:n.*175C=
ENST00000684214.1:c.485C= ENSP00000508071.1:p.Ala162=
ENST00000414835.7:c.560C= ENSP00000411960.3:p.Ala187=
ENST00000510025.7:c.485C= MANE Select ENSP00000424940.3:p.Ala162=
ENST00000643250.1:c.*357C= ENSP00000494737.1:n.*357C=
ENST00000644146.1:c.*63C= ENSP00000494808.1:n.*63C=
ENST00000645099.1:c.44C= ENSP00000496091.1:p.Ala15=
ENST00000645702.1:c.74C= ENSP00000496432.1:p.Ala25=
ENST00000645832.1:c.*370C= ENSP00000494316.1:n.*370C=
ENST00000646058.1:c.485C= ENSP00000493579.1:p.Ala162=
ENST00000646355.1:c.*491C= ENSP00000493801.1:n.*491C=
ENST00000646554.1:c.*463C= ENSP00000494542.1:n.*463C=
ENST00000646590.1:c.476C= ENSP00000494892.1:p.Ala159=
ENST00000647335.1:c.*452C= ENSP00000495180.1:n.*452C=
ENST00000647342.1:c.*416C= ENSP00000494992.1:n.*416C=
ENST00000256216.10:c.485C= ENSP00000256216.6:p.Ala162=
ENST00000414835.6:c.65C= ENSP00000411960.2:p.Ala22=
ENST00000442060.7:c.485C= ENSP00000390208.3:p.Ala162=
ENST00000503168.5:n.474C=
ENST00000504811.5:c.560C= ENSP00000420914.1:p.Ala187=
ENST00000505181.5:n.188C=
ENST00000508788.5:n.387C=
ENST00000509514.5:c.-400C= ENSP00000426272.1:n.-400C=
ENST00000510025.5:c.413C= ENSP00000424940.1:p.Ala138=
ENST00000512644.1:n.53C=
ENST00000512841.5:n.533C=
ENST00000513628.5:c.74C= ENSP00000425993.1:p.Ala25=
ENST00000515235.6:n.545C=
ENST00000515320.5:c.431C= ENSP00000424613.1:p.Ala144=
NM_000414.3:c.485C= NP_000405.1:p.Ala162=
NM_001199291.2:c.560C= NP_001186220.1:p.Ala187=
NM_001199292.1:c.431C= NP_001186221.1:p.Ala144=
NM_001292027.1:c.413C= NP_001278956.1:p.Ala138=
NM_001292028.1:c.65C= NP_001278957.1:p.Ala22=
NM_000414.4:c.485C= MANE Select NP_000405.1:p.Ala162=
NM_001199291.3:c.560C= NP_001186220.1:p.Ala187=
NM_001199292.2:c.431C= NP_001186221.1:p.Ala144=
NM_001292027.2:c.413C= NP_001278956.1:p.Ala138=
NM_001292028.2:c.65C= NP_001278957.1:p.Ala22=
NM_001374497.1:c.476C= NP_001361426.1:p.Ala159=
NM_001374498.1:c.485C= NP_001361427.1:p.Ala162=
NM_001374499.1:c.158C= NP_001361428.1:p.Ala53=
NM_001374500.1:c.44C= NP_001361429.1:p.Ala15=
NM_001374501.1:c.74C= NP_001361430.1:p.Ala25=
NM_001374502.1:c.74C= NP_001361431.1:p.Ala25=
NM_001374503.1:c.74C= NP_001361432.1:p.Ala25=
NR_164653.1:n.564C=
NR_164654.1:n.752C=