Canonical Allele Identifier: CA1577038591
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119514983A= , CM000667.2:g.119514983A= GRCh38
NC_000005.9:g.118850678A= , CM000667.1:g.118850678A= GRCh37
NC_000005.8:g.118878577A= NCBI36
NG_008182.1:g.67531A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1371A= ENSP00000426272.2:p.Val457=
ENST00000518349.6:c.684A= ENSP00000507185.1:p.Val228=
ENST00000520244.6:n.3178A=
ENST00000682445.1:c.*1321A= ENSP00000508061.1:n.*1321A=
ENST00000682531.1:n.3332A=
ENST00000682626.1:c.*946A= ENSP00000507857.1:n.*946A=
ENST00000682996.1:c.1368A= ENSP00000507792.1:p.Val456=
ENST00000683265.1:n.3226A=
ENST00000683335.1:n.2842A=
ENST00000683371.1:c.*1570A= ENSP00000508376.1:n.*1570A=
ENST00000683372.1:n.3450A=
ENST00000683390.1:n.3130A=
ENST00000683549.1:n.3054A=
ENST00000683936.1:c.*3018A= ENSP00000507721.1:n.*3018A=
ENST00000683974.1:n.3213-44A=
ENST00000683996.1:c.*650A= ENSP00000507060.1:n.*650A=
ENST00000684131.1:n.2972A=
ENST00000684160.1:c.*1130A= ENSP00000507821.1:n.*1130A=
ENST00000684214.1:c.1440A= ENSP00000508071.1:p.Val480=
ENST00000414835.7:c.1515A= ENSP00000411960.3:p.Val505=
ENST00000510025.7:c.1440A= MANE Select ENSP00000424940.3:p.Val480=
ENST00000643250.1:c.*1312A= ENSP00000494737.1:n.*1312A=
ENST00000644146.1:c.*2711A= ENSP00000494808.1:n.*2711A=
ENST00000645099.1:c.999A= ENSP00000496091.1:p.Val333=
ENST00000645702.1:c.*843A= ENSP00000496432.1:n.*843A=
ENST00000645832.1:c.*1325A= ENSP00000494316.1:n.*1325A=
ENST00000646058.1:c.1440A= ENSP00000493579.1:p.Val480=
ENST00000646355.1:c.*1446A= ENSP00000493801.1:n.*1446A=
ENST00000646554.1:c.*1418A= ENSP00000494542.1:n.*1418A=
ENST00000647335.1:c.*1407A= ENSP00000495180.1:n.*1407A=
ENST00000647342.1:c.*1371A= ENSP00000494992.1:n.*1371A=
ENST00000256216.10:c.1440A= ENSP00000256216.6:p.Val480=
ENST00000414835.6:c.1020A= ENSP00000411960.2:p.Val340=
ENST00000442060.7:c.*2A= ENSP00000390208.3:n.*2A=
ENST00000504811.5:c.1515A= ENSP00000420914.1:p.Val505=
ENST00000509514.5:c.654A= ENSP00000426272.1:p.Val218=
ENST00000510025.5:c.1368A= ENSP00000424940.1:p.Val456=
ENST00000513628.5:c.1029A= ENSP00000425993.1:p.Val343=
ENST00000515235.6:n.3193A=
ENST00000515320.5:c.1386A= ENSP00000424613.1:p.Val462=
ENST00000518349.5:n.574A=
ENST00000520244.5:n.223A=
ENST00000522415.5:n.107A=
NM_000414.3:c.1440A= NP_000405.1:p.Val480=
NM_001199291.2:c.1515A= NP_001186220.1:p.Val505=
NM_001199292.1:c.1386A= NP_001186221.1:p.Val462=
NM_001292027.1:c.1368A= NP_001278956.1:p.Val456=
NM_001292028.1:c.1020A= NP_001278957.1:p.Val340=
NM_000414.4:c.1440A= MANE Select NP_000405.1:p.Val480=
NM_001199291.3:c.1515A= NP_001186220.1:p.Val505=
NM_001199292.2:c.1386A= NP_001186221.1:p.Val462=
NM_001292027.2:c.1368A= NP_001278956.1:p.Val456=
NM_001292028.2:c.1020A= NP_001278957.1:p.Val340=
NM_001374497.1:c.1431A= NP_001361426.1:p.Val477=
NM_001374498.1:c.1368A= NP_001361427.1:p.Val456=
NM_001374499.1:c.1113A= NP_001361428.1:p.Val371=
NM_001374500.1:c.999A= NP_001361429.1:p.Val333=
NM_001374501.1:c.1029A= NP_001361430.1:p.Val343=
NM_001374502.1:c.1029A= NP_001361431.1:p.Val343=
NM_001374503.1:c.1029A= NP_001361432.1:p.Val343=
NR_164653.1:n.1537A=
NR_164654.1:n.1805A=