Canonical Allele Identifier: CA1577038595
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119514989A= , CM000667.2:g.119514989A= GRCh38
NC_000005.9:g.118850684A= , CM000667.1:g.118850684A= GRCh37
NC_000005.8:g.118878583A= NCBI36
NG_008182.1:g.67537A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.1377A= ENSP00000426272.2:p.Val459=
ENST00000518349.6:c.690A= ENSP00000507185.1:p.Val230=
ENST00000520244.6:n.3184A=
ENST00000682445.1:c.*1327A= ENSP00000508061.1:n.*1327A=
ENST00000682531.1:n.3338A=
ENST00000682626.1:c.*952A= ENSP00000507857.1:n.*952A=
ENST00000682996.1:c.1374A= ENSP00000507792.1:p.Val458=
ENST00000683265.1:n.3232A=
ENST00000683335.1:n.2848A=
ENST00000683371.1:c.*1576A= ENSP00000508376.1:n.*1576A=
ENST00000683372.1:n.3456A=
ENST00000683390.1:n.3136A=
ENST00000683549.1:n.3060A=
ENST00000683936.1:c.*3024A= ENSP00000507721.1:n.*3024A=
ENST00000683974.1:n.3213-38A=
ENST00000683996.1:c.*656A= ENSP00000507060.1:n.*656A=
ENST00000684131.1:n.2978A=
ENST00000684160.1:c.*1136A= ENSP00000507821.1:n.*1136A=
ENST00000684214.1:c.1446A= ENSP00000508071.1:p.Val482=
ENST00000414835.7:c.1521A= ENSP00000411960.3:p.Val507=
ENST00000510025.7:c.1446A= MANE Select ENSP00000424940.3:p.Val482=
ENST00000643250.1:c.*1318A= ENSP00000494737.1:n.*1318A=
ENST00000644146.1:c.*2717A= ENSP00000494808.1:n.*2717A=
ENST00000645099.1:c.1005A= ENSP00000496091.1:p.Val335=
ENST00000645702.1:c.*849A= ENSP00000496432.1:n.*849A=
ENST00000645832.1:c.*1331A= ENSP00000494316.1:n.*1331A=
ENST00000646058.1:c.1446A= ENSP00000493579.1:p.Val482=
ENST00000646355.1:c.*1452A= ENSP00000493801.1:n.*1452A=
ENST00000646554.1:c.*1424A= ENSP00000494542.1:n.*1424A=
ENST00000647335.1:c.*1413A= ENSP00000495180.1:n.*1413A=
ENST00000647342.1:c.*1377A= ENSP00000494992.1:n.*1377A=
ENST00000256216.10:c.1446A= ENSP00000256216.6:p.Val482=
ENST00000414835.6:c.1026A= ENSP00000411960.2:p.Val342=
ENST00000442060.7:c.*8A= ENSP00000390208.3:n.*8A=
ENST00000504811.5:c.1521A= ENSP00000420914.1:p.Val507=
ENST00000509514.5:c.660A= ENSP00000426272.1:p.Val220=
ENST00000510025.5:c.1374A= ENSP00000424940.1:p.Val458=
ENST00000513628.5:c.1035A= ENSP00000425993.1:p.Val345=
ENST00000515235.6:n.3199A=
ENST00000515320.5:c.1392A= ENSP00000424613.1:p.Val464=
ENST00000518349.5:n.580A=
ENST00000520244.5:n.229A=
ENST00000522415.5:n.113A=
NM_000414.3:c.1446A= NP_000405.1:p.Val482=
NM_001199291.2:c.1521A= NP_001186220.1:p.Val507=
NM_001199292.1:c.1392A= NP_001186221.1:p.Val464=
NM_001292027.1:c.1374A= NP_001278956.1:p.Val458=
NM_001292028.1:c.1026A= NP_001278957.1:p.Val342=
NM_000414.4:c.1446A= MANE Select NP_000405.1:p.Val482=
NM_001199291.3:c.1521A= NP_001186220.1:p.Val507=
NM_001199292.2:c.1392A= NP_001186221.1:p.Val464=
NM_001292027.2:c.1374A= NP_001278956.1:p.Val458=
NM_001292028.2:c.1026A= NP_001278957.1:p.Val342=
NM_001374497.1:c.1437A= NP_001361426.1:p.Val479=
NM_001374498.1:c.1374A= NP_001361427.1:p.Val458=
NM_001374499.1:c.1119A= NP_001361428.1:p.Val373=
NM_001374500.1:c.1005A= NP_001361429.1:p.Val335=
NM_001374501.1:c.1035A= NP_001361430.1:p.Val345=
NM_001374502.1:c.1035A= NP_001361431.1:p.Val345=
NM_001374503.1:c.1035A= NP_001361432.1:p.Val345=
NR_164653.1:n.1543A=
NR_164654.1:n.1811A=