Canonical Allele Identifier: CA2842509942
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478903del , CM000667.2:g.119478903del GRCh38
NC_000005.9:g.118814598del , CM000667.1:g.118814598del GRCh37
NC_000005.8:g.118842497del NCBI36
NG_008182.1:g.31451del

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.504del ENSP00000426272.2:p.Lys168AsnfsTer?
ENST00000518349.6:c.113-17640del ENSP00000507185.1:n.113-17640del
ENST00000682445.1:c.*385del ENSP00000508061.1:n.*385del
ENST00000682531.1:n.605del
ENST00000682626.1:c.*10del ENSP00000507857.1:n.*10del
ENST00000682996.1:c.504del ENSP00000507792.1:p.Lys168AsnfsTer?
ENST00000683265.1:n.597del
ENST00000683371.1:c.*634del ENSP00000508376.1:n.*634del
ENST00000683390.1:n.2194del
ENST00000683549.1:n.425del
ENST00000683936.1:c.*389del ENSP00000507721.1:n.*389del
ENST00000683974.1:n.586del
ENST00000683996.1:c.93del ENSP00000507060.1:p.Lys31AsnfsTer?
ENST00000684131.1:n.343del
ENST00000684160.1:c.*194del ENSP00000507821.1:n.*194del
ENST00000684214.1:c.504del ENSP00000508071.1:p.Lys168AsnfsTer?
ENST00000414835.7:c.579del ENSP00000411960.3:p.Lys193AsnfsTer?
ENST00000510025.7:c.504del MANE Select ENSP00000424940.3:p.Lys168AsnfsTer?
ENST00000643250.1:c.*376del ENSP00000494737.1:n.*376del
ENST00000644146.1:c.*82del ENSP00000494808.1:n.*82del
ENST00000645099.1:c.63del ENSP00000496091.1:p.Lys21AsnfsTer?
ENST00000645702.1:c.93del ENSP00000496432.1:p.Lys31AsnfsTer?
ENST00000645832.1:c.*389del ENSP00000494316.1:n.*389del
ENST00000646058.1:c.504del ENSP00000493579.1:p.Lys168AsnfsTer?
ENST00000646355.1:c.*510del ENSP00000493801.1:n.*510del
ENST00000646554.1:c.*482del ENSP00000494542.1:n.*482del
ENST00000646590.1:c.495del ENSP00000494892.1:p.Lys165AsnfsTer?
ENST00000647335.1:c.*471del ENSP00000495180.1:n.*471del
ENST00000647342.1:c.*435del ENSP00000494992.1:n.*435del
ENST00000256216.10:c.504del ENSP00000256216.6:p.Lys168AsnfsTer?
ENST00000414835.6:c.84del ENSP00000411960.2:p.Lys28AsnfsTer?
ENST00000442060.7:c.504del ENSP00000390208.3:p.Lys168AsnfsTer?
ENST00000503168.5:n.493del
ENST00000504811.5:c.579del ENSP00000420914.1:p.Lys193AsnfsTer?
ENST00000505181.5:n.207del
ENST00000508788.5:n.406del
ENST00000509514.5:c.-381del ENSP00000426272.1:n.-381del
ENST00000510025.5:c.432del ENSP00000424940.1:p.Lys144AsnfsTer?
ENST00000512644.1:n.72del
ENST00000512841.5:n.552del
ENST00000513628.5:c.93del ENSP00000425993.1:p.Lys31AsnfsTer?
ENST00000515235.6:n.564del
ENST00000515320.5:c.450del ENSP00000424613.1:p.Lys150AsnfsTer?
NM_000414.3:c.504del NP_000405.1:p.Lys168AsnfsTer?
NM_001199291.2:c.579del NP_001186220.1:p.Lys193AsnfsTer?
NM_001199292.1:c.450del NP_001186221.1:p.Lys150AsnfsTer?
NM_001292027.1:c.432del NP_001278956.1:p.Lys144AsnfsTer?
NM_001292028.1:c.84del NP_001278957.1:p.Lys28AsnfsTer?
NM_000414.4:c.504del MANE Select NP_000405.1:p.Lys168AsnfsTer?
NM_001199291.3:c.579del NP_001186220.1:p.Lys193AsnfsTer?
NM_001199292.2:c.450del NP_001186221.1:p.Lys150AsnfsTer?
NM_001292027.2:c.432del NP_001278956.1:p.Lys144AsnfsTer?
NM_001292028.2:c.84del NP_001278957.1:p.Lys28AsnfsTer?
NM_001374497.1:c.495del NP_001361426.1:p.Lys165AsnfsTer?
NM_001374498.1:c.504del NP_001361427.1:p.Lys168AsnfsTer?
NM_001374499.1:c.177del NP_001361428.1:p.Lys59AsnfsTer?
NM_001374500.1:c.63del NP_001361429.1:p.Lys21AsnfsTer?
NM_001374501.1:c.93del NP_001361430.1:p.Lys31AsnfsTer?
NM_001374502.1:c.93del NP_001361431.1:p.Lys31AsnfsTer?
NM_001374503.1:c.93del NP_001361432.1:p.Lys31AsnfsTer?
NR_164653.1:n.583del
NR_164654.1:n.771del