Canonical Allele Identifier: CA1577025571
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478904T= , CM000667.2:g.119478904T= GRCh38
NC_000005.9:g.118814599T= , CM000667.1:g.118814599T= GRCh37
NC_000005.8:g.118842498T= NCBI36
NG_008182.1:g.31452T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.505T= ENSP00000426272.2:p.Leu169=
ENST00000518349.6:c.113-17639T= ENSP00000507185.1:n.113-17639T=
ENST00000682445.1:c.*386T= ENSP00000508061.1:n.*386T=
ENST00000682531.1:n.606T=
ENST00000682626.1:c.*11T= ENSP00000507857.1:n.*11T=
ENST00000682996.1:c.505T= ENSP00000507792.1:p.Leu169=
ENST00000683265.1:n.598T=
ENST00000683371.1:c.*635T= ENSP00000508376.1:n.*635T=
ENST00000683390.1:n.2195T=
ENST00000683549.1:n.426T=
ENST00000683936.1:c.*390T= ENSP00000507721.1:n.*390T=
ENST00000683974.1:n.587T=
ENST00000683996.1:c.94T= ENSP00000507060.1:p.Leu32=
ENST00000684131.1:n.344T=
ENST00000684160.1:c.*195T= ENSP00000507821.1:n.*195T=
ENST00000684214.1:c.505T= ENSP00000508071.1:p.Leu169=
ENST00000414835.7:c.580T= ENSP00000411960.3:p.Leu194=
ENST00000510025.7:c.505T= MANE Select ENSP00000424940.3:p.Leu169=
ENST00000643250.1:c.*377T= ENSP00000494737.1:n.*377T=
ENST00000644146.1:c.*83T= ENSP00000494808.1:n.*83T=
ENST00000645099.1:c.64T= ENSP00000496091.1:p.Leu22=
ENST00000645702.1:c.94T= ENSP00000496432.1:p.Leu32=
ENST00000645832.1:c.*390T= ENSP00000494316.1:n.*390T=
ENST00000646058.1:c.505T= ENSP00000493579.1:p.Leu169=
ENST00000646355.1:c.*511T= ENSP00000493801.1:n.*511T=
ENST00000646554.1:c.*483T= ENSP00000494542.1:n.*483T=
ENST00000646590.1:c.496T= ENSP00000494892.1:p.Leu166=
ENST00000647335.1:c.*472T= ENSP00000495180.1:n.*472T=
ENST00000647342.1:c.*436T= ENSP00000494992.1:n.*436T=
ENST00000256216.10:c.505T= ENSP00000256216.6:p.Leu169=
ENST00000414835.6:c.85T= ENSP00000411960.2:p.Leu29=
ENST00000442060.7:c.505T= ENSP00000390208.3:p.Leu169=
ENST00000503168.5:n.494T=
ENST00000504811.5:c.580T= ENSP00000420914.1:p.Leu194=
ENST00000505181.5:n.208T=
ENST00000508788.5:n.407T=
ENST00000509514.5:c.-380T= ENSP00000426272.1:n.-380T=
ENST00000510025.5:c.433T= ENSP00000424940.1:p.Leu145=
ENST00000512644.1:n.73T=
ENST00000512841.5:n.553T=
ENST00000513628.5:c.94T= ENSP00000425993.1:p.Leu32=
ENST00000515235.6:n.565T=
ENST00000515320.5:c.451T= ENSP00000424613.1:p.Leu151=
NM_000414.3:c.505T= NP_000405.1:p.Leu169=
NM_001199291.2:c.580T= NP_001186220.1:p.Leu194=
NM_001199292.1:c.451T= NP_001186221.1:p.Leu151=
NM_001292027.1:c.433T= NP_001278956.1:p.Leu145=
NM_001292028.1:c.85T= NP_001278957.1:p.Leu29=
NM_000414.4:c.505T= MANE Select NP_000405.1:p.Leu169=
NM_001199291.3:c.580T= NP_001186220.1:p.Leu194=
NM_001199292.2:c.451T= NP_001186221.1:p.Leu151=
NM_001292027.2:c.433T= NP_001278956.1:p.Leu145=
NM_001292028.2:c.85T= NP_001278957.1:p.Leu29=
NM_001374497.1:c.496T= NP_001361426.1:p.Leu166=
NM_001374498.1:c.505T= NP_001361427.1:p.Leu169=
NM_001374499.1:c.178T= NP_001361428.1:p.Leu60=
NM_001374500.1:c.64T= NP_001361429.1:p.Leu22=
NM_001374501.1:c.94T= NP_001361430.1:p.Leu32=
NM_001374502.1:c.94T= NP_001361431.1:p.Leu32=
NM_001374503.1:c.94T= NP_001361432.1:p.Leu32=
NR_164653.1:n.584T=
NR_164654.1:n.772T=