Canonical Allele Identifier: CA1577025552
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478851C= , CM000667.2:g.119478851C= GRCh38
NC_000005.9:g.118814546C= , CM000667.1:g.118814546C= GRCh37
NC_000005.8:g.118842445C= NCBI36
NG_008182.1:g.31399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.452C= ENSP00000426272.2:p.Ser151=
ENST00000518349.6:c.113-17692C= ENSP00000507185.1:n.113-17692C=
ENST00000682445.1:c.*333C= ENSP00000508061.1:n.*333C=
ENST00000682531.1:n.553C=
ENST00000682626.1:c.480C= ENSP00000507857.1:p.Ile160=
ENST00000682996.1:c.452C= ENSP00000507792.1:p.Ser151=
ENST00000683265.1:n.545C=
ENST00000683371.1:c.*582C= ENSP00000508376.1:n.*582C=
ENST00000683390.1:n.2142C=
ENST00000683549.1:n.373C=
ENST00000683936.1:c.*337C= ENSP00000507721.1:n.*337C=
ENST00000683974.1:n.534C=
ENST00000683996.1:c.41C= ENSP00000507060.1:p.Ser14=
ENST00000684131.1:n.291C=
ENST00000684160.1:c.*142C= ENSP00000507821.1:n.*142C=
ENST00000684214.1:c.452C= ENSP00000508071.1:p.Ser151=
ENST00000414835.7:c.527C= ENSP00000411960.3:p.Ser176=
ENST00000510025.7:c.452C= MANE Select ENSP00000424940.3:p.Ser151=
ENST00000643250.1:c.*324C= ENSP00000494737.1:n.*324C=
ENST00000644146.1:c.*30C= ENSP00000494808.1:n.*30C=
ENST00000645099.1:c.11C= ENSP00000496091.1:p.Ser4=
ENST00000645702.1:c.41C= ENSP00000496432.1:p.Ser14=
ENST00000645832.1:c.*337C= ENSP00000494316.1:n.*337C=
ENST00000646058.1:c.452C= ENSP00000493579.1:p.Ser151=
ENST00000646355.1:c.*458C= ENSP00000493801.1:n.*458C=
ENST00000646554.1:c.*430C= ENSP00000494542.1:n.*430C=
ENST00000646590.1:c.443C= ENSP00000494892.1:p.Ser148=
ENST00000647335.1:c.*419C= ENSP00000495180.1:n.*419C=
ENST00000647342.1:c.*383C= ENSP00000494992.1:n.*383C=
ENST00000256216.10:c.452C= ENSP00000256216.6:p.Ser151=
ENST00000414835.6:c.32C= ENSP00000411960.2:p.Ser11=
ENST00000442060.7:c.452C= ENSP00000390208.3:p.Ser151=
ENST00000503168.5:n.441C=
ENST00000504811.5:c.527C= ENSP00000420914.1:p.Ser176=
ENST00000505181.5:n.155C=
ENST00000508788.5:n.354C=
ENST00000509514.5:c.-433C= ENSP00000426272.1:n.-433C=
ENST00000510025.5:c.380C= ENSP00000424940.1:p.Ser127=
ENST00000512644.1:n.20C=
ENST00000512841.5:n.500C=
ENST00000513628.5:c.41C= ENSP00000425993.1:p.Ser14=
ENST00000515235.6:n.512C=
ENST00000515320.5:c.398C= ENSP00000424613.1:p.Ser133=
NM_000414.3:c.452C= NP_000405.1:p.Ser151=
NM_001199291.2:c.527C= NP_001186220.1:p.Ser176=
NM_001199292.1:c.398C= NP_001186221.1:p.Ser133=
NM_001292027.1:c.380C= NP_001278956.1:p.Ser127=
NM_001292028.1:c.32C= NP_001278957.1:p.Ser11=
NM_000414.4:c.452C= MANE Select NP_000405.1:p.Ser151=
NM_001199291.3:c.527C= NP_001186220.1:p.Ser176=
NM_001199292.2:c.398C= NP_001186221.1:p.Ser133=
NM_001292027.2:c.380C= NP_001278956.1:p.Ser127=
NM_001292028.2:c.32C= NP_001278957.1:p.Ser11=
NM_001374497.1:c.443C= NP_001361426.1:p.Ser148=
NM_001374498.1:c.452C= NP_001361427.1:p.Ser151=
NM_001374499.1:c.125C= NP_001361428.1:p.Ser42=
NM_001374500.1:c.11C= NP_001361429.1:p.Ser4=
NM_001374501.1:c.41C= NP_001361430.1:p.Ser14=
NM_001374502.1:c.41C= NP_001361431.1:p.Ser14=
NM_001374503.1:c.41C= NP_001361432.1:p.Ser14=
NR_164653.1:n.531C=
NR_164654.1:n.719C=