Canonical Allele Identifier: CA1577025557
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478858A= , CM000667.2:g.119478858A= GRCh38
NC_000005.9:g.118814553A= , CM000667.1:g.118814553A= GRCh37
NC_000005.8:g.118842452A= NCBI36
NG_008182.1:g.31406A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.459A= ENSP00000426272.2:p.Ser153=
ENST00000518349.6:c.113-17685A= ENSP00000507185.1:n.113-17685A=
ENST00000682445.1:c.*340A= ENSP00000508061.1:n.*340A=
ENST00000682531.1:n.560A=
ENST00000682626.1:c.487A= ENSP00000507857.1:p.Arg163=
ENST00000682996.1:c.459A= ENSP00000507792.1:p.Ser153=
ENST00000683265.1:n.552A=
ENST00000683371.1:c.*589A= ENSP00000508376.1:n.*589A=
ENST00000683390.1:n.2149A=
ENST00000683549.1:n.380A=
ENST00000683936.1:c.*344A= ENSP00000507721.1:n.*344A=
ENST00000683974.1:n.541A=
ENST00000683996.1:c.48A= ENSP00000507060.1:p.Ser16=
ENST00000684131.1:n.298A=
ENST00000684160.1:c.*149A= ENSP00000507821.1:n.*149A=
ENST00000684214.1:c.459A= ENSP00000508071.1:p.Ser153=
ENST00000414835.7:c.534A= ENSP00000411960.3:p.Ser178=
ENST00000510025.7:c.459A= MANE Select ENSP00000424940.3:p.Ser153=
ENST00000643250.1:c.*331A= ENSP00000494737.1:n.*331A=
ENST00000644146.1:c.*37A= ENSP00000494808.1:n.*37A=
ENST00000645099.1:c.18A= ENSP00000496091.1:p.Ser6=
ENST00000645702.1:c.48A= ENSP00000496432.1:p.Ser16=
ENST00000645832.1:c.*344A= ENSP00000494316.1:n.*344A=
ENST00000646058.1:c.459A= ENSP00000493579.1:p.Ser153=
ENST00000646355.1:c.*465A= ENSP00000493801.1:n.*465A=
ENST00000646554.1:c.*437A= ENSP00000494542.1:n.*437A=
ENST00000646590.1:c.450A= ENSP00000494892.1:p.Ser150=
ENST00000647335.1:c.*426A= ENSP00000495180.1:n.*426A=
ENST00000647342.1:c.*390A= ENSP00000494992.1:n.*390A=
ENST00000256216.10:c.459A= ENSP00000256216.6:p.Ser153=
ENST00000414835.6:c.39A= ENSP00000411960.2:p.Ser13=
ENST00000442060.7:c.459A= ENSP00000390208.3:p.Ser153=
ENST00000503168.5:n.448A=
ENST00000504811.5:c.534A= ENSP00000420914.1:p.Ser178=
ENST00000505181.5:n.162A=
ENST00000508788.5:n.361A=
ENST00000509514.5:c.-426A= ENSP00000426272.1:n.-426A=
ENST00000510025.5:c.387A= ENSP00000424940.1:p.Ser129=
ENST00000512644.1:n.27A=
ENST00000512841.5:n.507A=
ENST00000513628.5:c.48A= ENSP00000425993.1:p.Ser16=
ENST00000515235.6:n.519A=
ENST00000515320.5:c.405A= ENSP00000424613.1:p.Ser135=
NM_000414.3:c.459A= NP_000405.1:p.Ser153=
NM_001199291.2:c.534A= NP_001186220.1:p.Ser178=
NM_001199292.1:c.405A= NP_001186221.1:p.Ser135=
NM_001292027.1:c.387A= NP_001278956.1:p.Ser129=
NM_001292028.1:c.39A= NP_001278957.1:p.Ser13=
NM_000414.4:c.459A= MANE Select NP_000405.1:p.Ser153=
NM_001199291.3:c.534A= NP_001186220.1:p.Ser178=
NM_001199292.2:c.405A= NP_001186221.1:p.Ser135=
NM_001292027.2:c.387A= NP_001278956.1:p.Ser129=
NM_001292028.2:c.39A= NP_001278957.1:p.Ser13=
NM_001374497.1:c.450A= NP_001361426.1:p.Ser150=
NM_001374498.1:c.459A= NP_001361427.1:p.Ser153=
NM_001374499.1:c.132A= NP_001361428.1:p.Ser44=
NM_001374500.1:c.18A= NP_001361429.1:p.Ser6=
NM_001374501.1:c.48A= NP_001361430.1:p.Ser16=
NM_001374502.1:c.48A= NP_001361431.1:p.Ser16=
NM_001374503.1:c.48A= NP_001361432.1:p.Ser16=
NR_164653.1:n.538A=
NR_164654.1:n.726A=