Canonical Allele Identifier: CA1577046981
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531356G= , CM000667.2:g.119531356G= GRCh38
NC_000005.9:g.118867051G= , CM000667.1:g.118867051G= GRCh37
NC_000005.8:g.118894950G= NCBI36
NG_008182.1:g.83904G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1876G= ENSP00000426272.2:p.Val626=
ENST00000518349.6:c.1189G= ENSP00000507185.1:p.Val397=
ENST00000682445.1:c.*1826G= ENSP00000508061.1:n.*1826G=
ENST00000682531.1:n.3837G=
ENST00000682626.1:c.*1451G= ENSP00000507857.1:n.*1451G=
ENST00000682996.1:c.1873G= ENSP00000507792.1:p.Val625=
ENST00000683265.1:n.3731G=
ENST00000683335.1:n.3347G=
ENST00000683371.1:c.*2075G= ENSP00000508376.1:n.*2075G=
ENST00000683372.1:n.3955G=
ENST00000683390.1:n.3635G=
ENST00000683476.1:n.787G=
ENST00000683549.1:n.3559G=
ENST00000683936.1:c.*3523G= ENSP00000507721.1:n.*3523G=
ENST00000683974.1:n.3674G=
ENST00000683996.1:c.*1155G= ENSP00000507060.1:n.*1155G=
ENST00000684131.1:n.3477G=
ENST00000684160.1:c.*1635G= ENSP00000507821.1:n.*1635G=
ENST00000684214.1:c.1854+1376G= ENSP00000508071.1:n.1854+1376G=
ENST00000414835.7:c.2020G= ENSP00000411960.3:p.Val674=
ENST00000510025.7:c.1945G= MANE Select ENSP00000424940.3:p.Val649=
ENST00000643250.1:c.*1817G= ENSP00000494737.1:n.*1817G=
ENST00000644146.1:c.*3216G= ENSP00000494808.1:n.*3216G=
ENST00000645099.1:c.1504G= ENSP00000496091.1:p.Val502=
ENST00000645702.1:c.*1348G= ENSP00000496432.1:n.*1348G=
ENST00000645832.1:c.*1830G= ENSP00000494316.1:n.*1830G=
ENST00000646058.1:c.1945G= ENSP00000493579.1:p.Val649=
ENST00000646355.1:c.*1951G= ENSP00000493801.1:n.*1951G=
ENST00000646554.1:c.*1923G= ENSP00000494542.1:n.*1923G=
ENST00000647335.1:c.*1912G= ENSP00000495180.1:n.*1912G=
ENST00000647342.1:c.*1876G= ENSP00000494992.1:n.*1876G=
ENST00000256216.10:c.1945G= ENSP00000256216.6:p.Val649=
ENST00000414835.6:c.1525G= ENSP00000411960.2:p.Val509=
ENST00000442060.7:c.*500G= ENSP00000390208.3:n.*500G=
ENST00000504811.5:c.2020G= ENSP00000420914.1:p.Val674=
ENST00000509514.5:c.1159G= ENSP00000426272.1:p.Val387=
ENST00000509606.1:n.240G=
ENST00000509951.5:n.309+1376G=
ENST00000510025.5:c.1873G= ENSP00000424940.1:p.Val625=
ENST00000513628.5:c.1534G= ENSP00000425993.1:p.Val512=
ENST00000515235.6:n.3698G=
ENST00000515320.5:c.1891G= ENSP00000424613.1:p.Val631=
ENST00000522415.5:n.612G=
NM_000414.3:c.1945G= NP_000405.1:p.Val649=
NM_001199291.2:c.2020G= NP_001186220.1:p.Val674=
NM_001199292.1:c.1891G= NP_001186221.1:p.Val631=
NM_001292027.1:c.1873G= NP_001278956.1:p.Val625=
NM_001292028.1:c.1525G= NP_001278957.1:p.Val509=
NM_000414.4:c.1945G= MANE Select NP_000405.1:p.Val649=
NM_001199291.3:c.2020G= NP_001186220.1:p.Val674=
NM_001199292.2:c.1891G= NP_001186221.1:p.Val631=
NM_001292027.2:c.1873G= NP_001278956.1:p.Val625=
NM_001292028.2:c.1525G= NP_001278957.1:p.Val509=
NM_001374497.1:c.1936G= NP_001361426.1:p.Val646=
NM_001374498.1:c.1873G= NP_001361427.1:p.Val625=
NM_001374499.1:c.1618G= NP_001361428.1:p.Val540=
NM_001374500.1:c.1504G= NP_001361429.1:p.Val502=
NM_001374501.1:c.1534G= NP_001361430.1:p.Val512=
NM_001374502.1:c.1534G= NP_001361431.1:p.Val512=
NM_001374503.1:c.1534G= NP_001361432.1:p.Val512=
NR_164653.1:n.2042G=
NR_164654.1:n.2310G=