Canonical Allele Identifier: CA360866110
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478860G>A , CM000667.2:g.119478860G>A GRCh38
NC_000005.9:g.118814555G>A , CM000667.1:g.118814555G>A GRCh37
NC_000005.8:g.118842454G>A NCBI36
NG_008182.1:g.31408G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.461G>A ENSP00000426272.2:p.Gly154Glu
ENST00000518349.6:c.113-17683G>A ENSP00000507185.1:n.113-17683G>A
ENST00000682445.1:c.*342G>A ENSP00000508061.1:n.*342G>A
ENST00000682531.1:n.562G>A
ENST00000682626.1:c.489G>A ENSP00000507857.1:p.Arg163=
ENST00000682996.1:c.461G>A ENSP00000507792.1:p.Gly154Glu
ENST00000683265.1:n.554G>A
ENST00000683371.1:c.*591G>A ENSP00000508376.1:n.*591G>A
ENST00000683390.1:n.2151G>A
ENST00000683549.1:n.382G>A
ENST00000683936.1:c.*346G>A ENSP00000507721.1:n.*346G>A
ENST00000683974.1:n.543G>A
ENST00000683996.1:c.50G>A ENSP00000507060.1:p.Gly17Glu
ENST00000684131.1:n.300G>A
ENST00000684160.1:c.*151G>A ENSP00000507821.1:n.*151G>A
ENST00000684214.1:c.461G>A ENSP00000508071.1:p.Gly154Glu
ENST00000414835.7:c.536G>A ENSP00000411960.3:p.Gly179Glu
ENST00000510025.7:c.461G>A MANE Select ENSP00000424940.3:p.Gly154Glu
ENST00000643250.1:c.*333G>A ENSP00000494737.1:n.*333G>A
ENST00000644146.1:c.*39G>A ENSP00000494808.1:n.*39G>A
ENST00000645099.1:c.20G>A ENSP00000496091.1:p.Gly7Glu
ENST00000645702.1:c.50G>A ENSP00000496432.1:p.Gly17Glu
ENST00000645832.1:c.*346G>A ENSP00000494316.1:n.*346G>A
ENST00000646058.1:c.461G>A ENSP00000493579.1:p.Gly154Glu
ENST00000646355.1:c.*467G>A ENSP00000493801.1:n.*467G>A
ENST00000646554.1:c.*439G>A ENSP00000494542.1:n.*439G>A
ENST00000646590.1:c.452G>A ENSP00000494892.1:p.Gly151Glu
ENST00000647335.1:c.*428G>A ENSP00000495180.1:n.*428G>A
ENST00000647342.1:c.*392G>A ENSP00000494992.1:n.*392G>A
ENST00000256216.10:c.461G>A ENSP00000256216.6:p.Gly154Glu
ENST00000414835.6:c.41G>A ENSP00000411960.2:p.Gly14Glu
ENST00000442060.7:c.461G>A ENSP00000390208.3:p.Gly154Glu
ENST00000503168.5:n.450G>A
ENST00000504811.5:c.536G>A ENSP00000420914.1:p.Gly179Glu
ENST00000505181.5:n.164G>A
ENST00000508788.5:n.363G>A
ENST00000509514.5:c.-424G>A ENSP00000426272.1:n.-424G>A
ENST00000510025.5:c.389G>A ENSP00000424940.1:p.Gly130Glu
ENST00000512644.1:n.29G>A
ENST00000512841.5:n.509G>A
ENST00000513628.5:c.50G>A ENSP00000425993.1:p.Gly17Glu
ENST00000515235.6:n.521G>A
ENST00000515320.5:c.407G>A ENSP00000424613.1:p.Gly136Glu
NM_000414.3:c.461G>A NP_000405.1:p.Gly154Glu
NM_001199291.2:c.536G>A NP_001186220.1:p.Gly179Glu
NM_001199292.1:c.407G>A NP_001186221.1:p.Gly136Glu
NM_001292027.1:c.389G>A NP_001278956.1:p.Gly130Glu
NM_001292028.1:c.41G>A NP_001278957.1:p.Gly14Glu
NM_000414.4:c.461G>A MANE Select NP_000405.1:p.Gly154Glu
NM_001199291.3:c.536G>A NP_001186220.1:p.Gly179Glu
NM_001199292.2:c.407G>A NP_001186221.1:p.Gly136Glu
NM_001292027.2:c.389G>A NP_001278956.1:p.Gly130Glu
NM_001292028.2:c.41G>A NP_001278957.1:p.Gly14Glu
NM_001374497.1:c.452G>A NP_001361426.1:p.Gly151Glu
NM_001374498.1:c.461G>A NP_001361427.1:p.Gly154Glu
NM_001374499.1:c.134G>A NP_001361428.1:p.Gly45Glu
NM_001374500.1:c.20G>A NP_001361429.1:p.Gly7Glu
NM_001374501.1:c.50G>A NP_001361430.1:p.Gly17Glu
NM_001374502.1:c.50G>A NP_001361431.1:p.Gly17Glu
NM_001374503.1:c.50G>A NP_001361432.1:p.Gly17Glu
NR_164653.1:n.540G>A
NR_164654.1:n.728G>A