Canonical Allele Identifier: CA1577030575
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119489194C= , CM000667.2:g.119489194C= GRCh38
NC_000005.9:g.118824889C= , CM000667.1:g.118824889C= GRCh37
NC_000005.8:g.118852788C= NCBI36
NG_008182.1:g.41742C=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.625C= ENSP00000426272.2:p.Leu209=
ENST00000518349.6:c.113-7349C= ENSP00000507185.1:n.113-7349C=
ENST00000682445.1:c.*506C= ENSP00000508061.1:n.*506C=
ENST00000682531.1:n.726C=
ENST00000682626.1:c.*131C= ENSP00000507857.1:n.*131C=
ENST00000682996.1:c.625C= ENSP00000507792.1:p.Leu209=
ENST00000683265.1:n.718C=
ENST00000683371.1:c.*755C= ENSP00000508376.1:n.*755C=
ENST00000683390.1:n.2315C=
ENST00000683549.1:n.546C=
ENST00000683936.1:c.*510C= ENSP00000507721.1:n.*510C=
ENST00000683974.1:n.707C=
ENST00000683996.1:c.214C= ENSP00000507060.1:p.Leu72=
ENST00000684131.1:n.464C=
ENST00000684160.1:c.*315C= ENSP00000507821.1:n.*315C=
ENST00000684214.1:c.625C= ENSP00000508071.1:p.Leu209=
ENST00000414835.7:c.700C= ENSP00000411960.3:p.Leu234=
ENST00000510025.7:c.625C= MANE Select ENSP00000424940.3:p.Leu209=
ENST00000643250.1:c.*497C= ENSP00000494737.1:n.*497C=
ENST00000644146.1:c.*203C= ENSP00000494808.1:n.*203C=
ENST00000645099.1:c.184C= ENSP00000496091.1:p.Leu62=
ENST00000645702.1:c.*28C= ENSP00000496432.1:n.*28C=
ENST00000645832.1:c.*510C= ENSP00000494316.1:n.*510C=
ENST00000646058.1:c.625C= ENSP00000493579.1:p.Leu209=
ENST00000646355.1:c.*631C= ENSP00000493801.1:n.*631C=
ENST00000646554.1:c.*603C= ENSP00000494542.1:n.*603C=
ENST00000647335.1:c.*592C= ENSP00000495180.1:n.*592C=
ENST00000647342.1:c.*556C= ENSP00000494992.1:n.*556C=
ENST00000256216.10:c.625C= ENSP00000256216.6:p.Leu209=
ENST00000414835.6:c.205C= ENSP00000411960.2:p.Leu69=
ENST00000442060.7:c.625C= ENSP00000390208.3:p.Leu209=
ENST00000504811.5:c.700C= ENSP00000420914.1:p.Leu234=
ENST00000505181.5:n.328C=
ENST00000509514.5:c.-260C= ENSP00000426272.1:n.-260C=
ENST00000510025.5:c.553C= ENSP00000424940.1:p.Leu185=
ENST00000512644.1:n.193C=
ENST00000513628.5:c.214C= ENSP00000425993.1:p.Leu72=
ENST00000515235.6:n.685C=
ENST00000515320.5:c.571C= ENSP00000424613.1:p.Leu191=
NM_000414.3:c.625C= NP_000405.1:p.Leu209=
NM_001199291.2:c.700C= NP_001186220.1:p.Leu234=
NM_001199292.1:c.571C= NP_001186221.1:p.Leu191=
NM_001292027.1:c.553C= NP_001278956.1:p.Leu185=
NM_001292028.1:c.205C= NP_001278957.1:p.Leu69=
NM_000414.4:c.625C= MANE Select NP_000405.1:p.Leu209=
NM_001199291.3:c.700C= NP_001186220.1:p.Leu234=
NM_001199292.2:c.571C= NP_001186221.1:p.Leu191=
NM_001292027.2:c.553C= NP_001278956.1:p.Leu185=
NM_001292028.2:c.205C= NP_001278957.1:p.Leu69=
NM_001374497.1:c.616C= NP_001361426.1:p.Leu206=
NM_001374498.1:c.625C= NP_001361427.1:p.Leu209=
NM_001374499.1:c.298C= NP_001361428.1:p.Leu100=
NM_001374500.1:c.184C= NP_001361429.1:p.Leu62=
NM_001374501.1:c.214C= NP_001361430.1:p.Leu72=
NM_001374502.1:c.214C= NP_001361431.1:p.Leu72=
NM_001374503.1:c.214C= NP_001361432.1:p.Leu72=
NR_164653.1:n.704C=
NR_164654.1:n.892C=