Canonical Allele Identifier: CA1577038614
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119515022T= , CM000667.2:g.119515022T= GRCh38
NC_000005.9:g.118850717T= , CM000667.1:g.118850717T= GRCh37
NC_000005.8:g.118878616T= NCBI36
NG_008182.1:g.67570T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1410T= ENSP00000426272.2:p.Leu470=
ENST00000518349.6:c.723T= ENSP00000507185.1:p.Leu241=
ENST00000520244.6:n.3217T=
ENST00000682445.1:c.*1360T= ENSP00000508061.1:n.*1360T=
ENST00000682531.1:n.3371T=
ENST00000682626.1:c.*985T= ENSP00000507857.1:n.*985T=
ENST00000682996.1:c.1407T= ENSP00000507792.1:p.Leu469=
ENST00000683265.1:n.3265T=
ENST00000683335.1:n.2881T=
ENST00000683371.1:c.*1609T= ENSP00000508376.1:n.*1609T=
ENST00000683372.1:n.3489T=
ENST00000683390.1:n.3169T=
ENST00000683549.1:n.3093T=
ENST00000683936.1:c.*3057T= ENSP00000507721.1:n.*3057T=
ENST00000683974.1:n.3213-5T=
ENST00000683996.1:c.*689T= ENSP00000507060.1:n.*689T=
ENST00000684131.1:n.3011T=
ENST00000684160.1:c.*1169T= ENSP00000507821.1:n.*1169T=
ENST00000684214.1:c.1479T= ENSP00000508071.1:p.Leu493=
ENST00000414835.7:c.1554T= ENSP00000411960.3:p.Leu518=
ENST00000510025.7:c.1479T= MANE Select ENSP00000424940.3:p.Leu493=
ENST00000643250.1:c.*1351T= ENSP00000494737.1:n.*1351T=
ENST00000644146.1:c.*2750T= ENSP00000494808.1:n.*2750T=
ENST00000645099.1:c.1038T= ENSP00000496091.1:p.Leu346=
ENST00000645702.1:c.*882T= ENSP00000496432.1:n.*882T=
ENST00000645832.1:c.*1364T= ENSP00000494316.1:n.*1364T=
ENST00000646058.1:c.1479T= ENSP00000493579.1:p.Leu493=
ENST00000646355.1:c.*1485T= ENSP00000493801.1:n.*1485T=
ENST00000646554.1:c.*1457T= ENSP00000494542.1:n.*1457T=
ENST00000647335.1:c.*1446T= ENSP00000495180.1:n.*1446T=
ENST00000647342.1:c.*1410T= ENSP00000494992.1:n.*1410T=
ENST00000256216.10:c.1479T= ENSP00000256216.6:p.Leu493=
ENST00000414835.6:c.1059T= ENSP00000411960.2:p.Leu353=
ENST00000442060.7:c.*41T= ENSP00000390208.3:n.*41T=
ENST00000504811.5:c.1554T= ENSP00000420914.1:p.Leu518=
ENST00000509514.5:c.693T= ENSP00000426272.1:p.Leu231=
ENST00000510025.5:c.1407T= ENSP00000424940.1:p.Leu469=
ENST00000513628.5:c.1068T= ENSP00000425993.1:p.Leu356=
ENST00000515235.6:n.3232T=
ENST00000515320.5:c.1425T= ENSP00000424613.1:p.Leu475=
ENST00000518349.5:n.613T=
ENST00000520244.5:n.262T=
ENST00000522415.5:n.146T=
NM_000414.3:c.1479T= NP_000405.1:p.Leu493=
NM_001199291.2:c.1554T= NP_001186220.1:p.Leu518=
NM_001199292.1:c.1425T= NP_001186221.1:p.Leu475=
NM_001292027.1:c.1407T= NP_001278956.1:p.Leu469=
NM_001292028.1:c.1059T= NP_001278957.1:p.Leu353=
NM_000414.4:c.1479T= MANE Select NP_000405.1:p.Leu493=
NM_001199291.3:c.1554T= NP_001186220.1:p.Leu518=
NM_001199292.2:c.1425T= NP_001186221.1:p.Leu475=
NM_001292027.2:c.1407T= NP_001278956.1:p.Leu469=
NM_001292028.2:c.1059T= NP_001278957.1:p.Leu353=
NM_001374497.1:c.1470T= NP_001361426.1:p.Leu490=
NM_001374498.1:c.1407T= NP_001361427.1:p.Leu469=
NM_001374499.1:c.1152T= NP_001361428.1:p.Leu384=
NM_001374500.1:c.1038T= NP_001361429.1:p.Leu346=
NM_001374501.1:c.1068T= NP_001361430.1:p.Leu356=
NM_001374502.1:c.1068T= NP_001361431.1:p.Leu356=
NM_001374503.1:c.1068T= NP_001361432.1:p.Leu356=
NR_164653.1:n.1576T=
NR_164654.1:n.1844T=