Canonical Allele Identifier: CA1577043845
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119525240G= , CM000667.2:g.119525240G= GRCh38
NC_000005.9:g.118860935G= , CM000667.1:g.118860935G= GRCh37
NC_000005.8:g.118888834G= NCBI36
NG_008182.1:g.77788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1459G= ENSP00000426272.2:p.Asp487=
ENST00000518349.6:c.772G= ENSP00000507185.1:p.Asp258=
ENST00000520244.6:n.3266G=
ENST00000682445.1:c.*1409G= ENSP00000508061.1:n.*1409G=
ENST00000682531.1:n.3420G=
ENST00000682626.1:c.*1034G= ENSP00000507857.1:n.*1034G=
ENST00000682996.1:c.1456G= ENSP00000507792.1:p.Asp486=
ENST00000683265.1:n.3314G=
ENST00000683335.1:n.2930G=
ENST00000683371.1:c.*1658G= ENSP00000508376.1:n.*1658G=
ENST00000683372.1:n.3538G=
ENST00000683390.1:n.3218G=
ENST00000683476.1:n.370G=
ENST00000683549.1:n.3142G=
ENST00000683936.1:c.*3106G= ENSP00000507721.1:n.*3106G=
ENST00000683974.1:n.3257G=
ENST00000683996.1:c.*738G= ENSP00000507060.1:n.*738G=
ENST00000684131.1:n.3060G=
ENST00000684160.1:c.*1218G= ENSP00000507821.1:n.*1218G=
ENST00000684214.1:c.1528G= ENSP00000508071.1:p.Asp510=
ENST00000414835.7:c.1603G= ENSP00000411960.3:p.Asp535=
ENST00000510025.7:c.1528G= MANE Select ENSP00000424940.3:p.Asp510=
ENST00000643250.1:c.*1400G= ENSP00000494737.1:n.*1400G=
ENST00000644146.1:c.*2799G= ENSP00000494808.1:n.*2799G=
ENST00000645099.1:c.1087G= ENSP00000496091.1:p.Asp363=
ENST00000645702.1:c.*931G= ENSP00000496432.1:n.*931G=
ENST00000645832.1:c.*1413G= ENSP00000494316.1:n.*1413G=
ENST00000646058.1:c.1528G= ENSP00000493579.1:p.Asp510=
ENST00000646355.1:c.*1534G= ENSP00000493801.1:n.*1534G=
ENST00000646554.1:c.*1506G= ENSP00000494542.1:n.*1506G=
ENST00000647335.1:c.*1495G= ENSP00000495180.1:n.*1495G=
ENST00000647342.1:c.*1459G= ENSP00000494992.1:n.*1459G=
ENST00000256216.10:c.1528G= ENSP00000256216.6:p.Asp510=
ENST00000414835.6:c.1108G= ENSP00000411960.2:p.Asp370=
ENST00000442060.7:c.*90G= ENSP00000390208.3:n.*90G=
ENST00000504811.5:c.1603G= ENSP00000420914.1:p.Asp535=
ENST00000509514.5:c.742G= ENSP00000426272.1:p.Asp248=
ENST00000510025.5:c.1456G= ENSP00000424940.1:p.Asp486=
ENST00000513628.5:c.1117G= ENSP00000425993.1:p.Asp373=
ENST00000515235.6:n.3281G=
ENST00000515320.5:c.1474G= ENSP00000424613.1:p.Asp492=
ENST00000518349.5:n.662G=
ENST00000520244.5:n.311G=
ENST00000522415.5:n.195G=
NM_000414.3:c.1528G= NP_000405.1:p.Asp510=
NM_001199291.2:c.1603G= NP_001186220.1:p.Asp535=
NM_001199292.1:c.1474G= NP_001186221.1:p.Asp492=
NM_001292027.1:c.1456G= NP_001278956.1:p.Asp486=
NM_001292028.1:c.1108G= NP_001278957.1:p.Asp370=
NM_000414.4:c.1528G= MANE Select NP_000405.1:p.Asp510=
NM_001199291.3:c.1603G= NP_001186220.1:p.Asp535=
NM_001199292.2:c.1474G= NP_001186221.1:p.Asp492=
NM_001292027.2:c.1456G= NP_001278956.1:p.Asp486=
NM_001292028.2:c.1108G= NP_001278957.1:p.Asp370=
NM_001374497.1:c.1519G= NP_001361426.1:p.Asp507=
NM_001374498.1:c.1456G= NP_001361427.1:p.Asp486=
NM_001374499.1:c.1201G= NP_001361428.1:p.Asp401=
NM_001374500.1:c.1087G= NP_001361429.1:p.Asp363=
NM_001374501.1:c.1117G= NP_001361430.1:p.Asp373=
NM_001374502.1:c.1117G= NP_001361431.1:p.Asp373=
NM_001374503.1:c.1117G= NP_001361432.1:p.Asp373=
NR_164653.1:n.1625G=
NR_164654.1:n.1893G=