Canonical Allele Identifier: CA1577025601
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478977C= , CM000667.2:g.119478977C= GRCh38
NC_000005.9:g.118814672C= , CM000667.1:g.118814672C= GRCh37
NC_000005.8:g.118842571C= NCBI36
NG_008182.1:g.31525C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.578C= ENSP00000426272.2:p.Ala193=
ENST00000518349.6:c.113-17566C= ENSP00000507185.1:n.113-17566C=
ENST00000682445.1:c.*459C= ENSP00000508061.1:n.*459C=
ENST00000682531.1:n.679C=
ENST00000682626.1:c.*84C= ENSP00000507857.1:n.*84C=
ENST00000682996.1:c.578C= ENSP00000507792.1:p.Ala193=
ENST00000683265.1:n.671C=
ENST00000683371.1:c.*708C= ENSP00000508376.1:n.*708C=
ENST00000683390.1:n.2268C=
ENST00000683549.1:n.499C=
ENST00000683936.1:c.*463C= ENSP00000507721.1:n.*463C=
ENST00000683974.1:n.660C=
ENST00000683996.1:c.167C= ENSP00000507060.1:p.Ala56=
ENST00000684131.1:n.417C=
ENST00000684160.1:c.*268C= ENSP00000507821.1:n.*268C=
ENST00000684214.1:c.578C= ENSP00000508071.1:p.Ala193=
ENST00000414835.7:c.653C= ENSP00000411960.3:p.Ala218=
ENST00000510025.7:c.578C= MANE Select ENSP00000424940.3:p.Ala193=
ENST00000643250.1:c.*450C= ENSP00000494737.1:n.*450C=
ENST00000644146.1:c.*156C= ENSP00000494808.1:n.*156C=
ENST00000645099.1:c.137C= ENSP00000496091.1:p.Ala46=
ENST00000645702.1:c.167C= ENSP00000496432.1:p.Ala56=
ENST00000645832.1:c.*463C= ENSP00000494316.1:n.*463C=
ENST00000646058.1:c.578C= ENSP00000493579.1:p.Ala193=
ENST00000646355.1:c.*584C= ENSP00000493801.1:n.*584C=
ENST00000646554.1:c.*556C= ENSP00000494542.1:n.*556C=
ENST00000647335.1:c.*545C= ENSP00000495180.1:n.*545C=
ENST00000647342.1:c.*509C= ENSP00000494992.1:n.*509C=
ENST00000256216.10:c.578C= ENSP00000256216.6:p.Ala193=
ENST00000414835.6:c.158C= ENSP00000411960.2:p.Ala53=
ENST00000442060.7:c.578C= ENSP00000390208.3:p.Ala193=
ENST00000503168.5:n.567C=
ENST00000504811.5:c.653C= ENSP00000420914.1:p.Ala218=
ENST00000505181.5:n.281C=
ENST00000509514.5:c.-307C= ENSP00000426272.1:n.-307C=
ENST00000510025.5:c.506C= ENSP00000424940.1:p.Ala169=
ENST00000512644.1:n.146C=
ENST00000513628.5:c.167C= ENSP00000425993.1:p.Ala56=
ENST00000515235.6:n.638C=
ENST00000515320.5:c.524C= ENSP00000424613.1:p.Ala175=
NM_000414.3:c.578C= NP_000405.1:p.Ala193=
NM_001199291.2:c.653C= NP_001186220.1:p.Ala218=
NM_001199292.1:c.524C= NP_001186221.1:p.Ala175=
NM_001292027.1:c.506C= NP_001278956.1:p.Ala169=
NM_001292028.1:c.158C= NP_001278957.1:p.Ala53=
NM_000414.4:c.578C= MANE Select NP_000405.1:p.Ala193=
NM_001199291.3:c.653C= NP_001186220.1:p.Ala218=
NM_001199292.2:c.524C= NP_001186221.1:p.Ala175=
NM_001292027.2:c.506C= NP_001278956.1:p.Ala169=
NM_001292028.2:c.158C= NP_001278957.1:p.Ala53=
NM_001374497.1:c.569C= NP_001361426.1:p.Ala190=
NM_001374498.1:c.578C= NP_001361427.1:p.Ala193=
NM_001374499.1:c.251C= NP_001361428.1:p.Ala84=
NM_001374500.1:c.137C= NP_001361429.1:p.Ala46=
NM_001374501.1:c.167C= NP_001361430.1:p.Ala56=
NM_001374502.1:c.167C= NP_001361431.1:p.Ala56=
NM_001374503.1:c.167C= NP_001361432.1:p.Ala56=
NR_164653.1:n.657C=
NR_164654.1:n.845C=