Canonical Allele Identifier: CA1577025578
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478922G= , CM000667.2:g.119478922G= GRCh38
NC_000005.9:g.118814617G= , CM000667.1:g.118814617G= GRCh37
NC_000005.8:g.118842516G= NCBI36
NG_008182.1:g.31470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.523G= ENSP00000426272.2:p.Ala175=
ENST00000518349.6:c.113-17621G= ENSP00000507185.1:n.113-17621G=
ENST00000682445.1:c.*404G= ENSP00000508061.1:n.*404G=
ENST00000682531.1:n.624G=
ENST00000682626.1:c.*29G= ENSP00000507857.1:n.*29G=
ENST00000682996.1:c.523G= ENSP00000507792.1:p.Ala175=
ENST00000683265.1:n.616G=
ENST00000683371.1:c.*653G= ENSP00000508376.1:n.*653G=
ENST00000683390.1:n.2213G=
ENST00000683549.1:n.444G=
ENST00000683936.1:c.*408G= ENSP00000507721.1:n.*408G=
ENST00000683974.1:n.605G=
ENST00000683996.1:c.112G= ENSP00000507060.1:p.Ala38=
ENST00000684131.1:n.362G=
ENST00000684160.1:c.*213G= ENSP00000507821.1:n.*213G=
ENST00000684214.1:c.523G= ENSP00000508071.1:p.Ala175=
ENST00000414835.7:c.598G= ENSP00000411960.3:p.Ala200=
ENST00000510025.7:c.523G= MANE Select ENSP00000424940.3:p.Ala175=
ENST00000643250.1:c.*395G= ENSP00000494737.1:n.*395G=
ENST00000644146.1:c.*101G= ENSP00000494808.1:n.*101G=
ENST00000645099.1:c.82G= ENSP00000496091.1:p.Ala28=
ENST00000645702.1:c.112G= ENSP00000496432.1:p.Ala38=
ENST00000645832.1:c.*408G= ENSP00000494316.1:n.*408G=
ENST00000646058.1:c.523G= ENSP00000493579.1:p.Ala175=
ENST00000646355.1:c.*529G= ENSP00000493801.1:n.*529G=
ENST00000646554.1:c.*501G= ENSP00000494542.1:n.*501G=
ENST00000647335.1:c.*490G= ENSP00000495180.1:n.*490G=
ENST00000647342.1:c.*454G= ENSP00000494992.1:n.*454G=
ENST00000256216.10:c.523G= ENSP00000256216.6:p.Ala175=
ENST00000414835.6:c.103G= ENSP00000411960.2:p.Ala35=
ENST00000442060.7:c.523G= ENSP00000390208.3:p.Ala175=
ENST00000503168.5:n.512G=
ENST00000504811.5:c.598G= ENSP00000420914.1:p.Ala200=
ENST00000505181.5:n.226G=
ENST00000508788.5:n.425G=
ENST00000509514.5:c.-362G= ENSP00000426272.1:n.-362G=
ENST00000510025.5:c.451G= ENSP00000424940.1:p.Ala151=
ENST00000512644.1:n.91G=
ENST00000512841.5:n.571G=
ENST00000513628.5:c.112G= ENSP00000425993.1:p.Ala38=
ENST00000515235.6:n.583G=
ENST00000515320.5:c.469G= ENSP00000424613.1:p.Ala157=
NM_000414.3:c.523G= NP_000405.1:p.Ala175=
NM_001199291.2:c.598G= NP_001186220.1:p.Ala200=
NM_001199292.1:c.469G= NP_001186221.1:p.Ala157=
NM_001292027.1:c.451G= NP_001278956.1:p.Ala151=
NM_001292028.1:c.103G= NP_001278957.1:p.Ala35=
NM_000414.4:c.523G= MANE Select NP_000405.1:p.Ala175=
NM_001199291.3:c.598G= NP_001186220.1:p.Ala200=
NM_001199292.2:c.469G= NP_001186221.1:p.Ala157=
NM_001292027.2:c.451G= NP_001278956.1:p.Ala151=
NM_001292028.2:c.103G= NP_001278957.1:p.Ala35=
NM_001374497.1:c.514G= NP_001361426.1:p.Ala172=
NM_001374498.1:c.523G= NP_001361427.1:p.Ala175=
NM_001374499.1:c.196G= NP_001361428.1:p.Ala66=
NM_001374500.1:c.82G= NP_001361429.1:p.Ala28=
NM_001374501.1:c.112G= NP_001361430.1:p.Ala38=
NM_001374502.1:c.112G= NP_001361431.1:p.Ala38=
NM_001374503.1:c.112G= NP_001361432.1:p.Ala38=
NR_164653.1:n.602G=
NR_164654.1:n.790G=