Canonical Allele Identifier: CA1577046964
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531325T= , CM000667.2:g.119531325T= GRCh38
NC_000005.9:g.118867020T= , CM000667.1:g.118867020T= GRCh37
NC_000005.8:g.118894919T= NCBI36
NG_008182.1:g.83873T=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.1845T= ENSP00000426272.2:p.Ile615=
ENST00000518349.6:c.1158T= ENSP00000507185.1:p.Ile386=
ENST00000682445.1:c.*1795T= ENSP00000508061.1:n.*1795T=
ENST00000682531.1:n.3806T=
ENST00000682626.1:c.*1420T= ENSP00000507857.1:n.*1420T=
ENST00000682996.1:c.1842T= ENSP00000507792.1:p.Ile614=
ENST00000683265.1:n.3700T=
ENST00000683335.1:n.3316T=
ENST00000683371.1:c.*2044T= ENSP00000508376.1:n.*2044T=
ENST00000683372.1:n.3924T=
ENST00000683390.1:n.3604T=
ENST00000683476.1:n.756T=
ENST00000683549.1:n.3528T=
ENST00000683936.1:c.*3492T= ENSP00000507721.1:n.*3492T=
ENST00000683974.1:n.3643T=
ENST00000683996.1:c.*1124T= ENSP00000507060.1:n.*1124T=
ENST00000684131.1:n.3446T=
ENST00000684160.1:c.*1604T= ENSP00000507821.1:n.*1604T=
ENST00000684214.1:c.1854+1345T= ENSP00000508071.1:n.1854+1345T=
ENST00000414835.7:c.1989T= ENSP00000411960.3:p.Ile663=
ENST00000510025.7:c.1914T= MANE Select ENSP00000424940.3:p.Ile638=
ENST00000643250.1:c.*1786T= ENSP00000494737.1:n.*1786T=
ENST00000644146.1:c.*3185T= ENSP00000494808.1:n.*3185T=
ENST00000645099.1:c.1473T= ENSP00000496091.1:p.Ile491=
ENST00000645702.1:c.*1317T= ENSP00000496432.1:n.*1317T=
ENST00000645832.1:c.*1799T= ENSP00000494316.1:n.*1799T=
ENST00000646058.1:c.1914T= ENSP00000493579.1:p.Ile638=
ENST00000646355.1:c.*1920T= ENSP00000493801.1:n.*1920T=
ENST00000646554.1:c.*1892T= ENSP00000494542.1:n.*1892T=
ENST00000647335.1:c.*1881T= ENSP00000495180.1:n.*1881T=
ENST00000647342.1:c.*1845T= ENSP00000494992.1:n.*1845T=
ENST00000256216.10:c.1914T= ENSP00000256216.6:p.Ile638=
ENST00000414835.6:c.1494T= ENSP00000411960.2:p.Ile498=
ENST00000442060.7:c.*469T= ENSP00000390208.3:n.*469T=
ENST00000504811.5:c.1989T= ENSP00000420914.1:p.Ile663=
ENST00000509514.5:c.1128T= ENSP00000426272.1:p.Ile376=
ENST00000509606.1:n.209T=
ENST00000509951.5:n.309+1345T=
ENST00000510025.5:c.1842T= ENSP00000424940.1:p.Ile614=
ENST00000513628.5:c.1503T= ENSP00000425993.1:p.Ile501=
ENST00000515235.6:n.3667T=
ENST00000515320.5:c.1860T= ENSP00000424613.1:p.Ile620=
ENST00000522415.5:n.581T=
NM_000414.3:c.1914T= NP_000405.1:p.Ile638=
NM_001199291.2:c.1989T= NP_001186220.1:p.Ile663=
NM_001199292.1:c.1860T= NP_001186221.1:p.Ile620=
NM_001292027.1:c.1842T= NP_001278956.1:p.Ile614=
NM_001292028.1:c.1494T= NP_001278957.1:p.Ile498=
NM_000414.4:c.1914T= MANE Select NP_000405.1:p.Ile638=
NM_001199291.3:c.1989T= NP_001186220.1:p.Ile663=
NM_001199292.2:c.1860T= NP_001186221.1:p.Ile620=
NM_001292027.2:c.1842T= NP_001278956.1:p.Ile614=
NM_001292028.2:c.1494T= NP_001278957.1:p.Ile498=
NM_001374497.1:c.1905T= NP_001361426.1:p.Ile635=
NM_001374498.1:c.1842T= NP_001361427.1:p.Ile614=
NM_001374499.1:c.1587T= NP_001361428.1:p.Ile529=
NM_001374500.1:c.1473T= NP_001361429.1:p.Ile491=
NM_001374501.1:c.1503T= NP_001361430.1:p.Ile501=
NM_001374502.1:c.1503T= NP_001361431.1:p.Ile501=
NM_001374503.1:c.1503T= NP_001361432.1:p.Ile501=
NR_164653.1:n.2011T=
NR_164654.1:n.2279T=