Canonical Allele Identifier: CA360866182
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478891T>A , CM000667.2:g.119478891T>A GRCh38
NC_000005.9:g.118814586T>A , CM000667.1:g.118814586T>A GRCh37
NC_000005.8:g.118842485T>A NCBI36
NG_008182.1:g.31439T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.492T>A ENSP00000426272.2:p.Tyr164Ter
ENST00000518349.6:c.113-17652T>A ENSP00000507185.1:n.113-17652T>A
ENST00000682445.1:c.*373T>A ENSP00000508061.1:n.*373T>A
ENST00000682531.1:n.593T>A
ENST00000682626.1:c.520T>A ENSP00000507857.1:p.Ter174Lys
ENST00000682996.1:c.492T>A ENSP00000507792.1:p.Tyr164Ter
ENST00000683265.1:n.585T>A
ENST00000683371.1:c.*622T>A ENSP00000508376.1:n.*622T>A
ENST00000683390.1:n.2182T>A
ENST00000683549.1:n.413T>A
ENST00000683936.1:c.*377T>A ENSP00000507721.1:n.*377T>A
ENST00000683974.1:n.574T>A
ENST00000683996.1:c.81T>A ENSP00000507060.1:p.Tyr27Ter
ENST00000684131.1:n.331T>A
ENST00000684160.1:c.*182T>A ENSP00000507821.1:n.*182T>A
ENST00000684214.1:c.492T>A ENSP00000508071.1:p.Tyr164Ter
ENST00000414835.7:c.567T>A ENSP00000411960.3:p.Tyr189Ter
ENST00000510025.7:c.492T>A MANE Select ENSP00000424940.3:p.Tyr164Ter
ENST00000643250.1:c.*364T>A ENSP00000494737.1:n.*364T>A
ENST00000644146.1:c.*70T>A ENSP00000494808.1:n.*70T>A
ENST00000645099.1:c.51T>A ENSP00000496091.1:p.Tyr17Ter
ENST00000645702.1:c.81T>A ENSP00000496432.1:p.Tyr27Ter
ENST00000645832.1:c.*377T>A ENSP00000494316.1:n.*377T>A
ENST00000646058.1:c.492T>A ENSP00000493579.1:p.Tyr164Ter
ENST00000646355.1:c.*498T>A ENSP00000493801.1:n.*498T>A
ENST00000646554.1:c.*470T>A ENSP00000494542.1:n.*470T>A
ENST00000646590.1:c.483T>A ENSP00000494892.1:p.Tyr161Ter
ENST00000647335.1:c.*459T>A ENSP00000495180.1:n.*459T>A
ENST00000647342.1:c.*423T>A ENSP00000494992.1:n.*423T>A
ENST00000256216.10:c.492T>A ENSP00000256216.6:p.Tyr164Ter
ENST00000414835.6:c.72T>A ENSP00000411960.2:p.Tyr24Ter
ENST00000442060.7:c.492T>A ENSP00000390208.3:p.Tyr164Ter
ENST00000503168.5:n.481T>A
ENST00000504811.5:c.567T>A ENSP00000420914.1:p.Tyr189Ter
ENST00000505181.5:n.195T>A
ENST00000508788.5:n.394T>A
ENST00000509514.5:c.-393T>A ENSP00000426272.1:n.-393T>A
ENST00000510025.5:c.420T>A ENSP00000424940.1:p.Tyr140Ter
ENST00000512644.1:n.60T>A
ENST00000512841.5:n.540T>A
ENST00000513628.5:c.81T>A ENSP00000425993.1:p.Tyr27Ter
ENST00000515235.6:n.552T>A
ENST00000515320.5:c.438T>A ENSP00000424613.1:p.Tyr146Ter
NM_000414.3:c.492T>A NP_000405.1:p.Tyr164Ter
NM_001199291.2:c.567T>A NP_001186220.1:p.Tyr189Ter
NM_001199292.1:c.438T>A NP_001186221.1:p.Tyr146Ter
NM_001292027.1:c.420T>A NP_001278956.1:p.Tyr140Ter
NM_001292028.1:c.72T>A NP_001278957.1:p.Tyr24Ter
NM_000414.4:c.492T>A MANE Select NP_000405.1:p.Tyr164Ter
NM_001199291.3:c.567T>A NP_001186220.1:p.Tyr189Ter
NM_001199292.2:c.438T>A NP_001186221.1:p.Tyr146Ter
NM_001292027.2:c.420T>A NP_001278956.1:p.Tyr140Ter
NM_001292028.2:c.72T>A NP_001278957.1:p.Tyr24Ter
NM_001374497.1:c.483T>A NP_001361426.1:p.Tyr161Ter
NM_001374498.1:c.492T>A NP_001361427.1:p.Tyr164Ter
NM_001374499.1:c.165T>A NP_001361428.1:p.Tyr55Ter
NM_001374500.1:c.51T>A NP_001361429.1:p.Tyr17Ter
NM_001374501.1:c.81T>A NP_001361430.1:p.Tyr27Ter
NM_001374502.1:c.81T>A NP_001361431.1:p.Tyr27Ter
NM_001374503.1:c.81T>A NP_001361432.1:p.Tyr27Ter
NR_164653.1:n.571T>A
NR_164654.1:n.759T>A