Canonical Allele Identifier: CA1577025558
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478861A= , CM000667.2:g.119478861A= GRCh38
NC_000005.9:g.118814556A= , CM000667.1:g.118814556A= GRCh37
NC_000005.8:g.118842455A= NCBI36
NG_008182.1:g.31409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.462A= ENSP00000426272.2:p.Gly154=
ENST00000518349.6:c.113-17682A= ENSP00000507185.1:n.113-17682A=
ENST00000682445.1:c.*343A= ENSP00000508061.1:n.*343A=
ENST00000682531.1:n.563A=
ENST00000682626.1:c.490A= ENSP00000507857.1:p.Asn164=
ENST00000682996.1:c.462A= ENSP00000507792.1:p.Gly154=
ENST00000683265.1:n.555A=
ENST00000683371.1:c.*592A= ENSP00000508376.1:n.*592A=
ENST00000683390.1:n.2152A=
ENST00000683549.1:n.383A=
ENST00000683936.1:c.*347A= ENSP00000507721.1:n.*347A=
ENST00000683974.1:n.544A=
ENST00000683996.1:c.51A= ENSP00000507060.1:p.Gly17=
ENST00000684131.1:n.301A=
ENST00000684160.1:c.*152A= ENSP00000507821.1:n.*152A=
ENST00000684214.1:c.462A= ENSP00000508071.1:p.Gly154=
ENST00000414835.7:c.537A= ENSP00000411960.3:p.Gly179=
ENST00000510025.7:c.462A= MANE Select ENSP00000424940.3:p.Gly154=
ENST00000643250.1:c.*334A= ENSP00000494737.1:n.*334A=
ENST00000644146.1:c.*40A= ENSP00000494808.1:n.*40A=
ENST00000645099.1:c.21A= ENSP00000496091.1:p.Gly7=
ENST00000645702.1:c.51A= ENSP00000496432.1:p.Gly17=
ENST00000645832.1:c.*347A= ENSP00000494316.1:n.*347A=
ENST00000646058.1:c.462A= ENSP00000493579.1:p.Gly154=
ENST00000646355.1:c.*468A= ENSP00000493801.1:n.*468A=
ENST00000646554.1:c.*440A= ENSP00000494542.1:n.*440A=
ENST00000646590.1:c.453A= ENSP00000494892.1:p.Gly151=
ENST00000647335.1:c.*429A= ENSP00000495180.1:n.*429A=
ENST00000647342.1:c.*393A= ENSP00000494992.1:n.*393A=
ENST00000256216.10:c.462A= ENSP00000256216.6:p.Gly154=
ENST00000414835.6:c.42A= ENSP00000411960.2:p.Gly14=
ENST00000442060.7:c.462A= ENSP00000390208.3:p.Gly154=
ENST00000503168.5:n.451A=
ENST00000504811.5:c.537A= ENSP00000420914.1:p.Gly179=
ENST00000505181.5:n.165A=
ENST00000508788.5:n.364A=
ENST00000509514.5:c.-423A= ENSP00000426272.1:n.-423A=
ENST00000510025.5:c.390A= ENSP00000424940.1:p.Gly130=
ENST00000512644.1:n.30A=
ENST00000512841.5:n.510A=
ENST00000513628.5:c.51A= ENSP00000425993.1:p.Gly17=
ENST00000515235.6:n.522A=
ENST00000515320.5:c.408A= ENSP00000424613.1:p.Gly136=
NM_000414.3:c.462A= NP_000405.1:p.Gly154=
NM_001199291.2:c.537A= NP_001186220.1:p.Gly179=
NM_001199292.1:c.408A= NP_001186221.1:p.Gly136=
NM_001292027.1:c.390A= NP_001278956.1:p.Gly130=
NM_001292028.1:c.42A= NP_001278957.1:p.Gly14=
NM_000414.4:c.462A= MANE Select NP_000405.1:p.Gly154=
NM_001199291.3:c.537A= NP_001186220.1:p.Gly179=
NM_001199292.2:c.408A= NP_001186221.1:p.Gly136=
NM_001292027.2:c.390A= NP_001278956.1:p.Gly130=
NM_001292028.2:c.42A= NP_001278957.1:p.Gly14=
NM_001374497.1:c.453A= NP_001361426.1:p.Gly151=
NM_001374498.1:c.462A= NP_001361427.1:p.Gly154=
NM_001374499.1:c.135A= NP_001361428.1:p.Gly45=
NM_001374500.1:c.21A= NP_001361429.1:p.Gly7=
NM_001374501.1:c.51A= NP_001361430.1:p.Gly17=
NM_001374502.1:c.51A= NP_001361431.1:p.Gly17=
NM_001374503.1:c.51A= NP_001361432.1:p.Gly17=
NR_164653.1:n.541A=
NR_164654.1:n.729A=