Canonical Allele Identifier: CA360866114
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478862A>G , CM000667.2:g.119478862A>G GRCh38
NC_000005.9:g.118814557A>G , CM000667.1:g.118814557A>G GRCh37
NC_000005.8:g.118842456A>G NCBI36
NG_008182.1:g.31410A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.463A>G ENSP00000426272.2:p.Ile155Val
ENST00000518349.6:c.113-17681A>G ENSP00000507185.1:n.113-17681A>G
ENST00000682445.1:c.*344A>G ENSP00000508061.1:n.*344A>G
ENST00000682531.1:n.564A>G
ENST00000682626.1:c.491A>G ENSP00000507857.1:p.Asn164Ser
ENST00000682996.1:c.463A>G ENSP00000507792.1:p.Ile155Val
ENST00000683265.1:n.556A>G
ENST00000683371.1:c.*593A>G ENSP00000508376.1:n.*593A>G
ENST00000683390.1:n.2153A>G
ENST00000683549.1:n.384A>G
ENST00000683936.1:c.*348A>G ENSP00000507721.1:n.*348A>G
ENST00000683974.1:n.545A>G
ENST00000683996.1:c.52A>G ENSP00000507060.1:p.Ile18Val
ENST00000684131.1:n.302A>G
ENST00000684160.1:c.*153A>G ENSP00000507821.1:n.*153A>G
ENST00000684214.1:c.463A>G ENSP00000508071.1:p.Ile155Val
ENST00000414835.7:c.538A>G ENSP00000411960.3:p.Ile180Val
ENST00000510025.7:c.463A>G MANE Select ENSP00000424940.3:p.Ile155Val
ENST00000643250.1:c.*335A>G ENSP00000494737.1:n.*335A>G
ENST00000644146.1:c.*41A>G ENSP00000494808.1:n.*41A>G
ENST00000645099.1:c.22A>G ENSP00000496091.1:p.Ile8Val
ENST00000645702.1:c.52A>G ENSP00000496432.1:p.Ile18Val
ENST00000645832.1:c.*348A>G ENSP00000494316.1:n.*348A>G
ENST00000646058.1:c.463A>G ENSP00000493579.1:p.Ile155Val
ENST00000646355.1:c.*469A>G ENSP00000493801.1:n.*469A>G
ENST00000646554.1:c.*441A>G ENSP00000494542.1:n.*441A>G
ENST00000646590.1:c.454A>G ENSP00000494892.1:p.Ile152Val
ENST00000647335.1:c.*430A>G ENSP00000495180.1:n.*430A>G
ENST00000647342.1:c.*394A>G ENSP00000494992.1:n.*394A>G
ENST00000256216.10:c.463A>G ENSP00000256216.6:p.Ile155Val
ENST00000414835.6:c.43A>G ENSP00000411960.2:p.Ile15Val
ENST00000442060.7:c.463A>G ENSP00000390208.3:p.Ile155Val
ENST00000503168.5:n.452A>G
ENST00000504811.5:c.538A>G ENSP00000420914.1:p.Ile180Val
ENST00000505181.5:n.166A>G
ENST00000508788.5:n.365A>G
ENST00000509514.5:c.-422A>G ENSP00000426272.1:n.-422A>G
ENST00000510025.5:c.391A>G ENSP00000424940.1:p.Ile131Val
ENST00000512644.1:n.31A>G
ENST00000512841.5:n.511A>G
ENST00000513628.5:c.52A>G ENSP00000425993.1:p.Ile18Val
ENST00000515235.6:n.523A>G
ENST00000515320.5:c.409A>G ENSP00000424613.1:p.Ile137Val
NM_000414.3:c.463A>G NP_000405.1:p.Ile155Val
NM_001199291.2:c.538A>G NP_001186220.1:p.Ile180Val
NM_001199292.1:c.409A>G NP_001186221.1:p.Ile137Val
NM_001292027.1:c.391A>G NP_001278956.1:p.Ile131Val
NM_001292028.1:c.43A>G NP_001278957.1:p.Ile15Val
NM_000414.4:c.463A>G MANE Select NP_000405.1:p.Ile155Val
NM_001199291.3:c.538A>G NP_001186220.1:p.Ile180Val
NM_001199292.2:c.409A>G NP_001186221.1:p.Ile137Val
NM_001292027.2:c.391A>G NP_001278956.1:p.Ile131Val
NM_001292028.2:c.43A>G NP_001278957.1:p.Ile15Val
NM_001374497.1:c.454A>G NP_001361426.1:p.Ile152Val
NM_001374498.1:c.463A>G NP_001361427.1:p.Ile155Val
NM_001374499.1:c.136A>G NP_001361428.1:p.Ile46Val
NM_001374500.1:c.22A>G NP_001361429.1:p.Ile8Val
NM_001374501.1:c.52A>G NP_001361430.1:p.Ile18Val
NM_001374502.1:c.52A>G NP_001361431.1:p.Ile18Val
NM_001374503.1:c.52A>G NP_001361432.1:p.Ile18Val
NR_164653.1:n.542A>G
NR_164654.1:n.730A>G