Canonical Allele Identifier: CA1577025553
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478852A= , CM000667.2:g.119478852A= GRCh38
NC_000005.9:g.118814547A= , CM000667.1:g.118814547A= GRCh37
NC_000005.8:g.118842446A= NCBI36
NG_008182.1:g.31400A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.453A= ENSP00000426272.2:p.Ser151=
ENST00000518349.6:c.113-17691A= ENSP00000507185.1:n.113-17691A=
ENST00000682445.1:c.*334A= ENSP00000508061.1:n.*334A=
ENST00000682531.1:n.554A=
ENST00000682626.1:c.481A= ENSP00000507857.1:p.Ser161=
ENST00000682996.1:c.453A= ENSP00000507792.1:p.Ser151=
ENST00000683265.1:n.546A=
ENST00000683371.1:c.*583A= ENSP00000508376.1:n.*583A=
ENST00000683390.1:n.2143A=
ENST00000683549.1:n.374A=
ENST00000683936.1:c.*338A= ENSP00000507721.1:n.*338A=
ENST00000683974.1:n.535A=
ENST00000683996.1:c.42A= ENSP00000507060.1:p.Ser14=
ENST00000684131.1:n.292A=
ENST00000684160.1:c.*143A= ENSP00000507821.1:n.*143A=
ENST00000684214.1:c.453A= ENSP00000508071.1:p.Ser151=
ENST00000414835.7:c.528A= ENSP00000411960.3:p.Ser176=
ENST00000510025.7:c.453A= MANE Select ENSP00000424940.3:p.Ser151=
ENST00000643250.1:c.*325A= ENSP00000494737.1:n.*325A=
ENST00000644146.1:c.*31A= ENSP00000494808.1:n.*31A=
ENST00000645099.1:c.12A= ENSP00000496091.1:p.Ser4=
ENST00000645702.1:c.42A= ENSP00000496432.1:p.Ser14=
ENST00000645832.1:c.*338A= ENSP00000494316.1:n.*338A=
ENST00000646058.1:c.453A= ENSP00000493579.1:p.Ser151=
ENST00000646355.1:c.*459A= ENSP00000493801.1:n.*459A=
ENST00000646554.1:c.*431A= ENSP00000494542.1:n.*431A=
ENST00000646590.1:c.444A= ENSP00000494892.1:p.Ser148=
ENST00000647335.1:c.*420A= ENSP00000495180.1:n.*420A=
ENST00000647342.1:c.*384A= ENSP00000494992.1:n.*384A=
ENST00000256216.10:c.453A= ENSP00000256216.6:p.Ser151=
ENST00000414835.6:c.33A= ENSP00000411960.2:p.Ser11=
ENST00000442060.7:c.453A= ENSP00000390208.3:p.Ser151=
ENST00000503168.5:n.442A=
ENST00000504811.5:c.528A= ENSP00000420914.1:p.Ser176=
ENST00000505181.5:n.156A=
ENST00000508788.5:n.355A=
ENST00000509514.5:c.-432A= ENSP00000426272.1:n.-432A=
ENST00000510025.5:c.381A= ENSP00000424940.1:p.Ser127=
ENST00000512644.1:n.21A=
ENST00000512841.5:n.501A=
ENST00000513628.5:c.42A= ENSP00000425993.1:p.Ser14=
ENST00000515235.6:n.513A=
ENST00000515320.5:c.399A= ENSP00000424613.1:p.Ser133=
NM_000414.3:c.453A= NP_000405.1:p.Ser151=
NM_001199291.2:c.528A= NP_001186220.1:p.Ser176=
NM_001199292.1:c.399A= NP_001186221.1:p.Ser133=
NM_001292027.1:c.381A= NP_001278956.1:p.Ser127=
NM_001292028.1:c.33A= NP_001278957.1:p.Ser11=
NM_000414.4:c.453A= MANE Select NP_000405.1:p.Ser151=
NM_001199291.3:c.528A= NP_001186220.1:p.Ser176=
NM_001199292.2:c.399A= NP_001186221.1:p.Ser133=
NM_001292027.2:c.381A= NP_001278956.1:p.Ser127=
NM_001292028.2:c.33A= NP_001278957.1:p.Ser11=
NM_001374497.1:c.444A= NP_001361426.1:p.Ser148=
NM_001374498.1:c.453A= NP_001361427.1:p.Ser151=
NM_001374499.1:c.126A= NP_001361428.1:p.Ser42=
NM_001374500.1:c.12A= NP_001361429.1:p.Ser4=
NM_001374501.1:c.42A= NP_001361430.1:p.Ser14=
NM_001374502.1:c.42A= NP_001361431.1:p.Ser14=
NM_001374503.1:c.42A= NP_001361432.1:p.Ser14=
NR_164653.1:n.532A=
NR_164654.1:n.720A=