Canonical Allele Identifier: CA1577025605
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478986C= , CM000667.2:g.119478986C= GRCh38
NC_000005.9:g.118814681C= , CM000667.1:g.118814681C= GRCh37
NC_000005.8:g.118842580C= NCBI36
NG_008182.1:g.31534C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.587C= ENSP00000426272.2:p.Ala196=
ENST00000518349.6:c.113-17557C= ENSP00000507185.1:n.113-17557C=
ENST00000682445.1:c.*468C= ENSP00000508061.1:n.*468C=
ENST00000682531.1:n.688C=
ENST00000682626.1:c.*93C= ENSP00000507857.1:n.*93C=
ENST00000682996.1:c.587C= ENSP00000507792.1:p.Ala196=
ENST00000683265.1:n.680C=
ENST00000683371.1:c.*717C= ENSP00000508376.1:n.*717C=
ENST00000683390.1:n.2277C=
ENST00000683549.1:n.508C=
ENST00000683936.1:c.*472C= ENSP00000507721.1:n.*472C=
ENST00000683974.1:n.669C=
ENST00000683996.1:c.176C= ENSP00000507060.1:p.Ala59=
ENST00000684131.1:n.426C=
ENST00000684160.1:c.*277C= ENSP00000507821.1:n.*277C=
ENST00000684214.1:c.587C= ENSP00000508071.1:p.Ala196=
ENST00000414835.7:c.662C= ENSP00000411960.3:p.Ala221=
ENST00000510025.7:c.587C= MANE Select ENSP00000424940.3:p.Ala196=
ENST00000643250.1:c.*459C= ENSP00000494737.1:n.*459C=
ENST00000644146.1:c.*165C= ENSP00000494808.1:n.*165C=
ENST00000645099.1:c.146C= ENSP00000496091.1:p.Ala49=
ENST00000645702.1:c.176C= ENSP00000496432.1:p.Ala59=
ENST00000645832.1:c.*472C= ENSP00000494316.1:n.*472C=
ENST00000646058.1:c.587C= ENSP00000493579.1:p.Ala196=
ENST00000646355.1:c.*593C= ENSP00000493801.1:n.*593C=
ENST00000646554.1:c.*565C= ENSP00000494542.1:n.*565C=
ENST00000647335.1:c.*554C= ENSP00000495180.1:n.*554C=
ENST00000647342.1:c.*518C= ENSP00000494992.1:n.*518C=
ENST00000256216.10:c.587C= ENSP00000256216.6:p.Ala196=
ENST00000414835.6:c.167C= ENSP00000411960.2:p.Ala56=
ENST00000442060.7:c.587C= ENSP00000390208.3:p.Ala196=
ENST00000503168.5:n.576C=
ENST00000504811.5:c.662C= ENSP00000420914.1:p.Ala221=
ENST00000505181.5:n.290C=
ENST00000509514.5:c.-298C= ENSP00000426272.1:n.-298C=
ENST00000510025.5:c.515C= ENSP00000424940.1:p.Ala172=
ENST00000512644.1:n.155C=
ENST00000513628.5:c.176C= ENSP00000425993.1:p.Ala59=
ENST00000515235.6:n.647C=
ENST00000515320.5:c.533C= ENSP00000424613.1:p.Ala178=
NM_000414.3:c.587C= NP_000405.1:p.Ala196=
NM_001199291.2:c.662C= NP_001186220.1:p.Ala221=
NM_001199292.1:c.533C= NP_001186221.1:p.Ala178=
NM_001292027.1:c.515C= NP_001278956.1:p.Ala172=
NM_001292028.1:c.167C= NP_001278957.1:p.Ala56=
NM_000414.4:c.587C= MANE Select NP_000405.1:p.Ala196=
NM_001199291.3:c.662C= NP_001186220.1:p.Ala221=
NM_001199292.2:c.533C= NP_001186221.1:p.Ala178=
NM_001292027.2:c.515C= NP_001278956.1:p.Ala172=
NM_001292028.2:c.167C= NP_001278957.1:p.Ala56=
NM_001374497.1:c.578C= NP_001361426.1:p.Ala193=
NM_001374498.1:c.587C= NP_001361427.1:p.Ala196=
NM_001374499.1:c.260C= NP_001361428.1:p.Ala87=
NM_001374500.1:c.146C= NP_001361429.1:p.Ala49=
NM_001374501.1:c.176C= NP_001361430.1:p.Ala59=
NM_001374502.1:c.176C= NP_001361431.1:p.Ala59=
NM_001374503.1:c.176C= NP_001361432.1:p.Ala59=
NR_164653.1:n.666C=
NR_164654.1:n.854C=