Canonical Allele Identifier: CA360871463
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531399A>G , CM000667.2:g.119531399A>G GRCh38
NC_000005.9:g.118867094A>G , CM000667.1:g.118867094A>G GRCh37
NC_000005.8:g.118894993A>G NCBI36
NG_008182.1:g.83947A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1919A>G ENSP00000426272.2:p.Lys640Arg
ENST00000518349.6:c.1232A>G ENSP00000507185.1:p.Lys411Arg
ENST00000682445.1:c.*1869A>G ENSP00000508061.1:n.*1869A>G
ENST00000682531.1:n.3880A>G
ENST00000682626.1:c.*1494A>G ENSP00000507857.1:n.*1494A>G
ENST00000682996.1:c.1916A>G ENSP00000507792.1:p.Lys639Arg
ENST00000683265.1:n.3774A>G
ENST00000683335.1:n.3390A>G
ENST00000683371.1:c.*2118A>G ENSP00000508376.1:n.*2118A>G
ENST00000683372.1:n.3998A>G
ENST00000683390.1:n.3678A>G
ENST00000683476.1:n.830A>G
ENST00000683549.1:n.3602A>G
ENST00000683936.1:c.*3566A>G ENSP00000507721.1:n.*3566A>G
ENST00000683974.1:n.3717A>G
ENST00000683996.1:c.*1198A>G ENSP00000507060.1:n.*1198A>G
ENST00000684131.1:n.3520A>G
ENST00000684160.1:c.*1678A>G ENSP00000507821.1:n.*1678A>G
ENST00000684214.1:c.1854+1419A>G ENSP00000508071.1:n.1854+1419A>G
ENST00000414835.7:c.2063A>G ENSP00000411960.3:p.Lys688Arg
ENST00000510025.7:c.1988A>G MANE Select ENSP00000424940.3:p.Lys663Arg
ENST00000643250.1:c.*1860A>G ENSP00000494737.1:n.*1860A>G
ENST00000644146.1:c.*3259A>G ENSP00000494808.1:n.*3259A>G
ENST00000645099.1:c.1547A>G ENSP00000496091.1:p.Lys516Arg
ENST00000645702.1:c.*1391A>G ENSP00000496432.1:n.*1391A>G
ENST00000645832.1:c.*1873A>G ENSP00000494316.1:n.*1873A>G
ENST00000646058.1:c.1988A>G ENSP00000493579.1:p.Lys663Arg
ENST00000646355.1:c.*1994A>G ENSP00000493801.1:n.*1994A>G
ENST00000646554.1:c.*1966A>G ENSP00000494542.1:n.*1966A>G
ENST00000647335.1:c.*1955A>G ENSP00000495180.1:n.*1955A>G
ENST00000647342.1:c.*1919A>G ENSP00000494992.1:n.*1919A>G
ENST00000256216.10:c.1988A>G ENSP00000256216.6:p.Lys663Arg
ENST00000414835.6:c.1568A>G ENSP00000411960.2:p.Lys523Arg
ENST00000442060.7:c.*543A>G ENSP00000390208.3:n.*543A>G
ENST00000504811.5:c.2063A>G ENSP00000420914.1:p.Lys688Arg
ENST00000509514.5:c.1202A>G ENSP00000426272.1:p.Lys401Arg
ENST00000509606.1:n.283A>G
ENST00000509951.5:n.309+1419A>G
ENST00000510025.5:c.1916A>G ENSP00000424940.1:p.Lys639Arg
ENST00000513628.5:c.1577A>G ENSP00000425993.1:p.Lys526Arg
ENST00000515235.6:n.3741A>G
ENST00000515320.5:c.1934A>G ENSP00000424613.1:p.Lys645Arg
ENST00000522415.5:n.655A>G
NM_000414.3:c.1988A>G NP_000405.1:p.Lys663Arg
NM_001199291.2:c.2063A>G NP_001186220.1:p.Lys688Arg
NM_001199292.1:c.1934A>G NP_001186221.1:p.Lys645Arg
NM_001292027.1:c.1916A>G NP_001278956.1:p.Lys639Arg
NM_001292028.1:c.1568A>G NP_001278957.1:p.Lys523Arg
NM_000414.4:c.1988A>G MANE Select NP_000405.1:p.Lys663Arg
NM_001199291.3:c.2063A>G NP_001186220.1:p.Lys688Arg
NM_001199292.2:c.1934A>G NP_001186221.1:p.Lys645Arg
NM_001292027.2:c.1916A>G NP_001278956.1:p.Lys639Arg
NM_001292028.2:c.1568A>G NP_001278957.1:p.Lys523Arg
NM_001374497.1:c.1979A>G NP_001361426.1:p.Lys660Arg
NM_001374498.1:c.1916A>G NP_001361427.1:p.Lys639Arg
NM_001374499.1:c.1661A>G NP_001361428.1:p.Lys554Arg
NM_001374500.1:c.1547A>G NP_001361429.1:p.Lys516Arg
NM_001374501.1:c.1577A>G NP_001361430.1:p.Lys526Arg
NM_001374502.1:c.1577A>G NP_001361431.1:p.Lys526Arg
NM_001374503.1:c.1577A>G NP_001361432.1:p.Lys526Arg
NR_164653.1:n.2085A>G
NR_164654.1:n.2353A>G