Canonical Allele Identifier: CA1577024053
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119475838G= , CM000667.2:g.119475838G= GRCh38
NC_000005.9:g.118811533G= , CM000667.1:g.118811533G= GRCh37
NC_000005.8:g.118839432G= NCBI36
NG_008182.1:g.28386G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.317G= ENSP00000426272.2:p.Arg106=
ENST00000518349.6:c.112+19470G= ENSP00000507185.1:n.112+19470G=
ENST00000682445.1:c.*198G= ENSP00000508061.1:n.*198G=
ENST00000682531.1:n.418G=
ENST00000682626.1:c.377+111G= ENSP00000507857.1:n.377+111G=
ENST00000682996.1:c.317G= ENSP00000507792.1:p.Arg106=
ENST00000683265.1:n.410G=
ENST00000683371.1:c.*447G= ENSP00000508376.1:n.*447G=
ENST00000683390.1:n.461G=
ENST00000683936.1:c.*202G= ENSP00000507721.1:n.*202G=
ENST00000683974.1:n.399G=
ENST00000684160.1:c.392G= ENSP00000507821.1:p.Arg131=
ENST00000684214.1:c.317G= ENSP00000508071.1:p.Arg106=
ENST00000414835.7:c.392G= ENSP00000411960.3:p.Arg131=
ENST00000510025.7:c.317G= MANE Select ENSP00000424940.3:p.Arg106=
ENST00000643250.1:c.*198G= ENSP00000494737.1:n.*198G=
ENST00000644146.1:c.317G= ENSP00000494808.1:p.Arg106=
ENST00000645832.1:c.*202G= ENSP00000494316.1:n.*202G=
ENST00000646058.1:c.317G= ENSP00000493579.1:p.Arg106=
ENST00000646355.1:c.*323G= ENSP00000493801.1:n.*323G=
ENST00000646554.1:c.*198G= ENSP00000494542.1:n.*198G=
ENST00000646590.1:c.317G= ENSP00000494892.1:p.Arg106=
ENST00000647335.1:c.*284G= ENSP00000495180.1:n.*284G=
ENST00000647342.1:c.*198G= ENSP00000494992.1:n.*198G=
ENST00000256216.10:c.317G= ENSP00000256216.6:p.Arg106=
ENST00000414835.6:c.-95G= ENSP00000411960.2:n.-95G=
ENST00000442060.7:c.317G= ENSP00000390208.3:p.Arg106=
ENST00000503168.5:n.306G=
ENST00000504811.5:c.392G= ENSP00000420914.1:p.Arg131=
ENST00000507695.1:n.289G=
ENST00000510025.5:c.245G= ENSP00000424940.1:p.Arg82=
ENST00000511186.5:n.448G=
ENST00000512841.5:n.365G=
ENST00000515235.6:n.377G=
ENST00000515320.5:c.263G= ENSP00000424613.1:p.Arg88=
NM_000414.3:c.317G= NP_000405.1:p.Arg106=
NM_001199291.2:c.392G= NP_001186220.1:p.Arg131=
NM_001199292.1:c.263G= NP_001186221.1:p.Arg88=
NM_001292027.1:c.245G= NP_001278956.1:p.Arg82=
NM_001292028.1:c.-95G= NP_001278957.1:n.-95G=
NM_000414.4:c.317G= MANE Select NP_000405.1:p.Arg106=
NM_001199291.3:c.392G= NP_001186220.1:p.Arg131=
NM_001199292.2:c.263G= NP_001186221.1:p.Arg88=
NM_001292027.2:c.245G= NP_001278956.1:p.Arg82=
NM_001292028.2:c.-95G= NP_001278957.1:n.-95G=
NM_001374497.1:c.317G= NP_001361426.1:p.Arg106=
NM_001374498.1:c.317G= NP_001361427.1:p.Arg106=
NM_001374499.1:c.22+111G= NP_001361428.1:n.22+111G=
NM_001374500.1:c.-222G= NP_001361429.1:n.-222G=
NM_001374501.1:c.-95G= NP_001361430.1:n.-95G=
NM_001374502.1:c.-95G= NP_001361431.1:n.-95G=
NM_001374503.1:c.-95G= NP_001361432.1:n.-95G=
NR_164653.1:n.396G=
NR_164654.1:n.584G=