Canonical Allele Identifier: CA360866151
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478877G>C , CM000667.2:g.119478877G>C GRCh38
NC_000005.9:g.118814572G>C , CM000667.1:g.118814572G>C GRCh37
NC_000005.8:g.118842471G>C NCBI36
NG_008182.1:g.31425G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.478G>C ENSP00000426272.2:p.Gly160Arg
ENST00000518349.6:c.113-17666G>C ENSP00000507185.1:n.113-17666G>C
ENST00000682445.1:c.*359G>C ENSP00000508061.1:n.*359G>C
ENST00000682531.1:n.579G>C
ENST00000682626.1:c.506G>C ENSP00000507857.1:p.Trp169Ser
ENST00000682996.1:c.478G>C ENSP00000507792.1:p.Gly160Arg
ENST00000683265.1:n.571G>C
ENST00000683371.1:c.*608G>C ENSP00000508376.1:n.*608G>C
ENST00000683390.1:n.2168G>C
ENST00000683549.1:n.399G>C
ENST00000683936.1:c.*363G>C ENSP00000507721.1:n.*363G>C
ENST00000683974.1:n.560G>C
ENST00000683996.1:c.67G>C ENSP00000507060.1:p.Gly23Arg
ENST00000684131.1:n.317G>C
ENST00000684160.1:c.*168G>C ENSP00000507821.1:n.*168G>C
ENST00000684214.1:c.478G>C ENSP00000508071.1:p.Gly160Arg
ENST00000414835.7:c.553G>C ENSP00000411960.3:p.Gly185Arg
ENST00000510025.7:c.478G>C MANE Select ENSP00000424940.3:p.Gly160Arg
ENST00000643250.1:c.*350G>C ENSP00000494737.1:n.*350G>C
ENST00000644146.1:c.*56G>C ENSP00000494808.1:n.*56G>C
ENST00000645099.1:c.37G>C ENSP00000496091.1:p.Gly13Arg
ENST00000645702.1:c.67G>C ENSP00000496432.1:p.Gly23Arg
ENST00000645832.1:c.*363G>C ENSP00000494316.1:n.*363G>C
ENST00000646058.1:c.478G>C ENSP00000493579.1:p.Gly160Arg
ENST00000646355.1:c.*484G>C ENSP00000493801.1:n.*484G>C
ENST00000646554.1:c.*456G>C ENSP00000494542.1:n.*456G>C
ENST00000646590.1:c.469G>C ENSP00000494892.1:p.Gly157Arg
ENST00000647335.1:c.*445G>C ENSP00000495180.1:n.*445G>C
ENST00000647342.1:c.*409G>C ENSP00000494992.1:n.*409G>C
ENST00000256216.10:c.478G>C ENSP00000256216.6:p.Gly160Arg
ENST00000414835.6:c.58G>C ENSP00000411960.2:p.Gly20Arg
ENST00000442060.7:c.478G>C ENSP00000390208.3:p.Gly160Arg
ENST00000503168.5:n.467G>C
ENST00000504811.5:c.553G>C ENSP00000420914.1:p.Gly185Arg
ENST00000505181.5:n.181G>C
ENST00000508788.5:n.380G>C
ENST00000509514.5:c.-407G>C ENSP00000426272.1:n.-407G>C
ENST00000510025.5:c.406G>C ENSP00000424940.1:p.Gly136Arg
ENST00000512644.1:n.46G>C
ENST00000512841.5:n.526G>C
ENST00000513628.5:c.67G>C ENSP00000425993.1:p.Gly23Arg
ENST00000515235.6:n.538G>C
ENST00000515320.5:c.424G>C ENSP00000424613.1:p.Gly142Arg
NM_000414.3:c.478G>C NP_000405.1:p.Gly160Arg
NM_001199291.2:c.553G>C NP_001186220.1:p.Gly185Arg
NM_001199292.1:c.424G>C NP_001186221.1:p.Gly142Arg
NM_001292027.1:c.406G>C NP_001278956.1:p.Gly136Arg
NM_001292028.1:c.58G>C NP_001278957.1:p.Gly20Arg
NM_000414.4:c.478G>C MANE Select NP_000405.1:p.Gly160Arg
NM_001199291.3:c.553G>C NP_001186220.1:p.Gly185Arg
NM_001199292.2:c.424G>C NP_001186221.1:p.Gly142Arg
NM_001292027.2:c.406G>C NP_001278956.1:p.Gly136Arg
NM_001292028.2:c.58G>C NP_001278957.1:p.Gly20Arg
NM_001374497.1:c.469G>C NP_001361426.1:p.Gly157Arg
NM_001374498.1:c.478G>C NP_001361427.1:p.Gly160Arg
NM_001374499.1:c.151G>C NP_001361428.1:p.Gly51Arg
NM_001374500.1:c.37G>C NP_001361429.1:p.Gly13Arg
NM_001374501.1:c.67G>C NP_001361430.1:p.Gly23Arg
NM_001374502.1:c.67G>C NP_001361431.1:p.Gly23Arg
NM_001374503.1:c.67G>C NP_001361432.1:p.Gly23Arg
NR_164653.1:n.557G>C
NR_164654.1:n.745G>C