Canonical Allele Identifier: CA1577043857
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119525259T= , CM000667.2:g.119525259T= GRCh38
NC_000005.9:g.118860954T= , CM000667.1:g.118860954T= GRCh37
NC_000005.8:g.118888853T= NCBI36
NG_008182.1:g.77807T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1478T= ENSP00000426272.2:p.Ile493=
ENST00000518349.6:c.791T= ENSP00000507185.1:p.Ile264=
ENST00000520244.6:n.3285T=
ENST00000682445.1:c.*1428T= ENSP00000508061.1:n.*1428T=
ENST00000682531.1:n.3439T=
ENST00000682626.1:c.*1053T= ENSP00000507857.1:n.*1053T=
ENST00000682996.1:c.1475T= ENSP00000507792.1:p.Ile492=
ENST00000683265.1:n.3333T=
ENST00000683335.1:n.2949T=
ENST00000683371.1:c.*1677T= ENSP00000508376.1:n.*1677T=
ENST00000683372.1:n.3557T=
ENST00000683390.1:n.3237T=
ENST00000683476.1:n.389T=
ENST00000683549.1:n.3161T=
ENST00000683936.1:c.*3125T= ENSP00000507721.1:n.*3125T=
ENST00000683974.1:n.3276T=
ENST00000683996.1:c.*757T= ENSP00000507060.1:n.*757T=
ENST00000684131.1:n.3079T=
ENST00000684160.1:c.*1237T= ENSP00000507821.1:n.*1237T=
ENST00000684214.1:c.1547T= ENSP00000508071.1:p.Ile516=
ENST00000414835.7:c.1622T= ENSP00000411960.3:p.Ile541=
ENST00000510025.7:c.1547T= MANE Select ENSP00000424940.3:p.Ile516=
ENST00000643250.1:c.*1419T= ENSP00000494737.1:n.*1419T=
ENST00000644146.1:c.*2818T= ENSP00000494808.1:n.*2818T=
ENST00000645099.1:c.1106T= ENSP00000496091.1:p.Ile369=
ENST00000645702.1:c.*950T= ENSP00000496432.1:n.*950T=
ENST00000645832.1:c.*1432T= ENSP00000494316.1:n.*1432T=
ENST00000646058.1:c.1547T= ENSP00000493579.1:p.Ile516=
ENST00000646355.1:c.*1553T= ENSP00000493801.1:n.*1553T=
ENST00000646554.1:c.*1525T= ENSP00000494542.1:n.*1525T=
ENST00000647335.1:c.*1514T= ENSP00000495180.1:n.*1514T=
ENST00000647342.1:c.*1478T= ENSP00000494992.1:n.*1478T=
ENST00000256216.10:c.1547T= ENSP00000256216.6:p.Ile516=
ENST00000414835.6:c.1127T= ENSP00000411960.2:p.Ile376=
ENST00000442060.7:c.*109T= ENSP00000390208.3:n.*109T=
ENST00000504811.5:c.1622T= ENSP00000420914.1:p.Ile541=
ENST00000509514.5:c.761T= ENSP00000426272.1:p.Ile254=
ENST00000509951.5:n.2T=
ENST00000510025.5:c.1475T= ENSP00000424940.1:p.Ile492=
ENST00000513628.5:c.1136T= ENSP00000425993.1:p.Ile379=
ENST00000515235.6:n.3300T=
ENST00000515320.5:c.1493T= ENSP00000424613.1:p.Ile498=
ENST00000518349.5:n.681T=
ENST00000520244.5:n.330T=
ENST00000522415.5:n.214T=
NM_000414.3:c.1547T= NP_000405.1:p.Ile516=
NM_001199291.2:c.1622T= NP_001186220.1:p.Ile541=
NM_001199292.1:c.1493T= NP_001186221.1:p.Ile498=
NM_001292027.1:c.1475T= NP_001278956.1:p.Ile492=
NM_001292028.1:c.1127T= NP_001278957.1:p.Ile376=
NM_000414.4:c.1547T= MANE Select NP_000405.1:p.Ile516=
NM_001199291.3:c.1622T= NP_001186220.1:p.Ile541=
NM_001199292.2:c.1493T= NP_001186221.1:p.Ile498=
NM_001292027.2:c.1475T= NP_001278956.1:p.Ile492=
NM_001292028.2:c.1127T= NP_001278957.1:p.Ile376=
NM_001374497.1:c.1538T= NP_001361426.1:p.Ile513=
NM_001374498.1:c.1475T= NP_001361427.1:p.Ile492=
NM_001374499.1:c.1220T= NP_001361428.1:p.Ile407=
NM_001374500.1:c.1106T= NP_001361429.1:p.Ile369=
NM_001374501.1:c.1136T= NP_001361430.1:p.Ile379=
NM_001374502.1:c.1136T= NP_001361431.1:p.Ile379=
NM_001374503.1:c.1136T= NP_001361432.1:p.Ile379=
NR_164653.1:n.1644T=
NR_164654.1:n.1912T=