Canonical Allele Identifier: CA1577025565
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478887A= , CM000667.2:g.119478887A= GRCh38
NC_000005.9:g.118814582A= , CM000667.1:g.118814582A= GRCh37
NC_000005.8:g.118842481A= NCBI36
NG_008182.1:g.31435A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.488A= ENSP00000426272.2:p.Asn163=
ENST00000518349.6:c.113-17656A= ENSP00000507185.1:n.113-17656A=
ENST00000682445.1:c.*369A= ENSP00000508061.1:n.*369A=
ENST00000682531.1:n.589A=
ENST00000682626.1:c.516A= ENSP00000507857.1:p.Gln172=
ENST00000682996.1:c.488A= ENSP00000507792.1:p.Asn163=
ENST00000683265.1:n.581A=
ENST00000683371.1:c.*618A= ENSP00000508376.1:n.*618A=
ENST00000683390.1:n.2178A=
ENST00000683549.1:n.409A=
ENST00000683936.1:c.*373A= ENSP00000507721.1:n.*373A=
ENST00000683974.1:n.570A=
ENST00000683996.1:c.77A= ENSP00000507060.1:p.Asn26=
ENST00000684131.1:n.327A=
ENST00000684160.1:c.*178A= ENSP00000507821.1:n.*178A=
ENST00000684214.1:c.488A= ENSP00000508071.1:p.Asn163=
ENST00000414835.7:c.563A= ENSP00000411960.3:p.Asn188=
ENST00000510025.7:c.488A= MANE Select ENSP00000424940.3:p.Asn163=
ENST00000643250.1:c.*360A= ENSP00000494737.1:n.*360A=
ENST00000644146.1:c.*66A= ENSP00000494808.1:n.*66A=
ENST00000645099.1:c.47A= ENSP00000496091.1:p.Asn16=
ENST00000645702.1:c.77A= ENSP00000496432.1:p.Asn26=
ENST00000645832.1:c.*373A= ENSP00000494316.1:n.*373A=
ENST00000646058.1:c.488A= ENSP00000493579.1:p.Asn163=
ENST00000646355.1:c.*494A= ENSP00000493801.1:n.*494A=
ENST00000646554.1:c.*466A= ENSP00000494542.1:n.*466A=
ENST00000646590.1:c.479A= ENSP00000494892.1:p.Asn160=
ENST00000647335.1:c.*455A= ENSP00000495180.1:n.*455A=
ENST00000647342.1:c.*419A= ENSP00000494992.1:n.*419A=
ENST00000256216.10:c.488A= ENSP00000256216.6:p.Asn163=
ENST00000414835.6:c.68A= ENSP00000411960.2:p.Asn23=
ENST00000442060.7:c.488A= ENSP00000390208.3:p.Asn163=
ENST00000503168.5:n.477A=
ENST00000504811.5:c.563A= ENSP00000420914.1:p.Asn188=
ENST00000505181.5:n.191A=
ENST00000508788.5:n.390A=
ENST00000509514.5:c.-397A= ENSP00000426272.1:n.-397A=
ENST00000510025.5:c.416A= ENSP00000424940.1:p.Asn139=
ENST00000512644.1:n.56A=
ENST00000512841.5:n.536A=
ENST00000513628.5:c.77A= ENSP00000425993.1:p.Asn26=
ENST00000515235.6:n.548A=
ENST00000515320.5:c.434A= ENSP00000424613.1:p.Asn145=
NM_000414.3:c.488A= NP_000405.1:p.Asn163=
NM_001199291.2:c.563A= NP_001186220.1:p.Asn188=
NM_001199292.1:c.434A= NP_001186221.1:p.Asn145=
NM_001292027.1:c.416A= NP_001278956.1:p.Asn139=
NM_001292028.1:c.68A= NP_001278957.1:p.Asn23=
NM_000414.4:c.488A= MANE Select NP_000405.1:p.Asn163=
NM_001199291.3:c.563A= NP_001186220.1:p.Asn188=
NM_001199292.2:c.434A= NP_001186221.1:p.Asn145=
NM_001292027.2:c.416A= NP_001278956.1:p.Asn139=
NM_001292028.2:c.68A= NP_001278957.1:p.Asn23=
NM_001374497.1:c.479A= NP_001361426.1:p.Asn160=
NM_001374498.1:c.488A= NP_001361427.1:p.Asn163=
NM_001374499.1:c.161A= NP_001361428.1:p.Asn54=
NM_001374500.1:c.47A= NP_001361429.1:p.Asn16=
NM_001374501.1:c.77A= NP_001361430.1:p.Asn26=
NM_001374502.1:c.77A= NP_001361431.1:p.Asn26=
NM_001374503.1:c.77A= NP_001361432.1:p.Asn26=
NR_164653.1:n.567A=
NR_164654.1:n.755A=