Canonical Allele Identifier: CA1577038589
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119514981G= , CM000667.2:g.119514981G= GRCh38
NC_000005.9:g.118850676G= , CM000667.1:g.118850676G= GRCh37
NC_000005.8:g.118878575G= NCBI36
NG_008182.1:g.67529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1369G= ENSP00000426272.2:p.Val457=
ENST00000518349.6:c.682G= ENSP00000507185.1:p.Val228=
ENST00000520244.6:n.3176G=
ENST00000682445.1:c.*1319G= ENSP00000508061.1:n.*1319G=
ENST00000682531.1:n.3330G=
ENST00000682626.1:c.*944G= ENSP00000507857.1:n.*944G=
ENST00000682996.1:c.1366G= ENSP00000507792.1:p.Val456=
ENST00000683265.1:n.3224G=
ENST00000683335.1:n.2840G=
ENST00000683371.1:c.*1568G= ENSP00000508376.1:n.*1568G=
ENST00000683372.1:n.3448G=
ENST00000683390.1:n.3128G=
ENST00000683549.1:n.3052G=
ENST00000683936.1:c.*3016G= ENSP00000507721.1:n.*3016G=
ENST00000683974.1:n.3213-46G=
ENST00000683996.1:c.*648G= ENSP00000507060.1:n.*648G=
ENST00000684131.1:n.2970G=
ENST00000684160.1:c.*1128G= ENSP00000507821.1:n.*1128G=
ENST00000684214.1:c.1438G= ENSP00000508071.1:p.Val480=
ENST00000414835.7:c.1513G= ENSP00000411960.3:p.Val505=
ENST00000510025.7:c.1438G= MANE Select ENSP00000424940.3:p.Val480=
ENST00000643250.1:c.*1310G= ENSP00000494737.1:n.*1310G=
ENST00000644146.1:c.*2709G= ENSP00000494808.1:n.*2709G=
ENST00000645099.1:c.997G= ENSP00000496091.1:p.Val333=
ENST00000645702.1:c.*841G= ENSP00000496432.1:n.*841G=
ENST00000645832.1:c.*1323G= ENSP00000494316.1:n.*1323G=
ENST00000646058.1:c.1438G= ENSP00000493579.1:p.Val480=
ENST00000646355.1:c.*1444G= ENSP00000493801.1:n.*1444G=
ENST00000646554.1:c.*1416G= ENSP00000494542.1:n.*1416G=
ENST00000647335.1:c.*1405G= ENSP00000495180.1:n.*1405G=
ENST00000647342.1:c.*1369G= ENSP00000494992.1:n.*1369G=
ENST00000256216.10:c.1438G= ENSP00000256216.6:p.Val480=
ENST00000414835.6:c.1018G= ENSP00000411960.2:p.Val340=
ENST00000442060.7:c.1503G= ENSP00000390208.3:p.Ter501=
ENST00000504811.5:c.1513G= ENSP00000420914.1:p.Val505=
ENST00000509514.5:c.652G= ENSP00000426272.1:p.Val218=
ENST00000510025.5:c.1366G= ENSP00000424940.1:p.Val456=
ENST00000513628.5:c.1027G= ENSP00000425993.1:p.Val343=
ENST00000515235.6:n.3191G=
ENST00000515320.5:c.1384G= ENSP00000424613.1:p.Val462=
ENST00000518349.5:n.572G=
ENST00000520244.5:n.221G=
ENST00000522415.5:n.105G=
NM_000414.3:c.1438G= NP_000405.1:p.Val480=
NM_001199291.2:c.1513G= NP_001186220.1:p.Val505=
NM_001199292.1:c.1384G= NP_001186221.1:p.Val462=
NM_001292027.1:c.1366G= NP_001278956.1:p.Val456=
NM_001292028.1:c.1018G= NP_001278957.1:p.Val340=
NM_000414.4:c.1438G= MANE Select NP_000405.1:p.Val480=
NM_001199291.3:c.1513G= NP_001186220.1:p.Val505=
NM_001199292.2:c.1384G= NP_001186221.1:p.Val462=
NM_001292027.2:c.1366G= NP_001278956.1:p.Val456=
NM_001292028.2:c.1018G= NP_001278957.1:p.Val340=
NM_001374497.1:c.1429G= NP_001361426.1:p.Val477=
NM_001374498.1:c.1366G= NP_001361427.1:p.Val456=
NM_001374499.1:c.1111G= NP_001361428.1:p.Val371=
NM_001374500.1:c.997G= NP_001361429.1:p.Val333=
NM_001374501.1:c.1027G= NP_001361430.1:p.Val343=
NM_001374502.1:c.1027G= NP_001361431.1:p.Val343=
NM_001374503.1:c.1027G= NP_001361432.1:p.Val343=
NR_164653.1:n.1535G=
NR_164654.1:n.1803G=