Canonical Allele Identifier: CA1577025600
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478976G= , CM000667.2:g.119478976G= GRCh38
NC_000005.9:g.118814671G= , CM000667.1:g.118814671G= GRCh37
NC_000005.8:g.118842570G= NCBI36
NG_008182.1:g.31524G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.577G= ENSP00000426272.2:p.Ala193=
ENST00000518349.6:c.113-17567G= ENSP00000507185.1:n.113-17567G=
ENST00000682445.1:c.*458G= ENSP00000508061.1:n.*458G=
ENST00000682531.1:n.678G=
ENST00000682626.1:c.*83G= ENSP00000507857.1:n.*83G=
ENST00000682996.1:c.577G= ENSP00000507792.1:p.Ala193=
ENST00000683265.1:n.670G=
ENST00000683371.1:c.*707G= ENSP00000508376.1:n.*707G=
ENST00000683390.1:n.2267G=
ENST00000683549.1:n.498G=
ENST00000683936.1:c.*462G= ENSP00000507721.1:n.*462G=
ENST00000683974.1:n.659G=
ENST00000683996.1:c.166G= ENSP00000507060.1:p.Ala56=
ENST00000684131.1:n.416G=
ENST00000684160.1:c.*267G= ENSP00000507821.1:n.*267G=
ENST00000684214.1:c.577G= ENSP00000508071.1:p.Ala193=
ENST00000414835.7:c.652G= ENSP00000411960.3:p.Ala218=
ENST00000510025.7:c.577G= MANE Select ENSP00000424940.3:p.Ala193=
ENST00000643250.1:c.*449G= ENSP00000494737.1:n.*449G=
ENST00000644146.1:c.*155G= ENSP00000494808.1:n.*155G=
ENST00000645099.1:c.136G= ENSP00000496091.1:p.Ala46=
ENST00000645702.1:c.166G= ENSP00000496432.1:p.Ala56=
ENST00000645832.1:c.*462G= ENSP00000494316.1:n.*462G=
ENST00000646058.1:c.577G= ENSP00000493579.1:p.Ala193=
ENST00000646355.1:c.*583G= ENSP00000493801.1:n.*583G=
ENST00000646554.1:c.*555G= ENSP00000494542.1:n.*555G=
ENST00000647335.1:c.*544G= ENSP00000495180.1:n.*544G=
ENST00000647342.1:c.*508G= ENSP00000494992.1:n.*508G=
ENST00000256216.10:c.577G= ENSP00000256216.6:p.Ala193=
ENST00000414835.6:c.157G= ENSP00000411960.2:p.Ala53=
ENST00000442060.7:c.577G= ENSP00000390208.3:p.Ala193=
ENST00000503168.5:n.566G=
ENST00000504811.5:c.652G= ENSP00000420914.1:p.Ala218=
ENST00000505181.5:n.280G=
ENST00000509514.5:c.-308G= ENSP00000426272.1:n.-308G=
ENST00000510025.5:c.505G= ENSP00000424940.1:p.Ala169=
ENST00000512644.1:n.145G=
ENST00000513628.5:c.166G= ENSP00000425993.1:p.Ala56=
ENST00000515235.6:n.637G=
ENST00000515320.5:c.523G= ENSP00000424613.1:p.Ala175=
NM_000414.3:c.577G= NP_000405.1:p.Ala193=
NM_001199291.2:c.652G= NP_001186220.1:p.Ala218=
NM_001199292.1:c.523G= NP_001186221.1:p.Ala175=
NM_001292027.1:c.505G= NP_001278956.1:p.Ala169=
NM_001292028.1:c.157G= NP_001278957.1:p.Ala53=
NM_000414.4:c.577G= MANE Select NP_000405.1:p.Ala193=
NM_001199291.3:c.652G= NP_001186220.1:p.Ala218=
NM_001199292.2:c.523G= NP_001186221.1:p.Ala175=
NM_001292027.2:c.505G= NP_001278956.1:p.Ala169=
NM_001292028.2:c.157G= NP_001278957.1:p.Ala53=
NM_001374497.1:c.568G= NP_001361426.1:p.Ala190=
NM_001374498.1:c.577G= NP_001361427.1:p.Ala193=
NM_001374499.1:c.250G= NP_001361428.1:p.Ala84=
NM_001374500.1:c.136G= NP_001361429.1:p.Ala46=
NM_001374501.1:c.166G= NP_001361430.1:p.Ala56=
NM_001374502.1:c.166G= NP_001361431.1:p.Ala56=
NM_001374503.1:c.166G= NP_001361432.1:p.Ala56=
NR_164653.1:n.656G=
NR_164654.1:n.844G=