Canonical Allele Identifier: CA360871370
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531377A>T , CM000667.2:g.119531377A>T GRCh38
NC_000005.9:g.118867072A>T , CM000667.1:g.118867072A>T GRCh37
NC_000005.8:g.118894971A>T NCBI36
NG_008182.1:g.83925A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1897A>T ENSP00000426272.2:p.Lys633Ter
ENST00000518349.6:c.1210A>T ENSP00000507185.1:p.Lys404Ter
ENST00000682445.1:c.*1847A>T ENSP00000508061.1:n.*1847A>T
ENST00000682531.1:n.3858A>T
ENST00000682626.1:c.*1472A>T ENSP00000507857.1:n.*1472A>T
ENST00000682996.1:c.1894A>T ENSP00000507792.1:p.Lys632Ter
ENST00000683265.1:n.3752A>T
ENST00000683335.1:n.3368A>T
ENST00000683371.1:c.*2096A>T ENSP00000508376.1:n.*2096A>T
ENST00000683372.1:n.3976A>T
ENST00000683390.1:n.3656A>T
ENST00000683476.1:n.808A>T
ENST00000683549.1:n.3580A>T
ENST00000683936.1:c.*3544A>T ENSP00000507721.1:n.*3544A>T
ENST00000683974.1:n.3695A>T
ENST00000683996.1:c.*1176A>T ENSP00000507060.1:n.*1176A>T
ENST00000684131.1:n.3498A>T
ENST00000684160.1:c.*1656A>T ENSP00000507821.1:n.*1656A>T
ENST00000684214.1:c.1854+1397A>T ENSP00000508071.1:n.1854+1397A>T
ENST00000414835.7:c.2041A>T ENSP00000411960.3:p.Lys681Ter
ENST00000510025.7:c.1966A>T MANE Select ENSP00000424940.3:p.Lys656Ter
ENST00000643250.1:c.*1838A>T ENSP00000494737.1:n.*1838A>T
ENST00000644146.1:c.*3237A>T ENSP00000494808.1:n.*3237A>T
ENST00000645099.1:c.1525A>T ENSP00000496091.1:p.Lys509Ter
ENST00000645702.1:c.*1369A>T ENSP00000496432.1:n.*1369A>T
ENST00000645832.1:c.*1851A>T ENSP00000494316.1:n.*1851A>T
ENST00000646058.1:c.1966A>T ENSP00000493579.1:p.Lys656Ter
ENST00000646355.1:c.*1972A>T ENSP00000493801.1:n.*1972A>T
ENST00000646554.1:c.*1944A>T ENSP00000494542.1:n.*1944A>T
ENST00000647335.1:c.*1933A>T ENSP00000495180.1:n.*1933A>T
ENST00000647342.1:c.*1897A>T ENSP00000494992.1:n.*1897A>T
ENST00000256216.10:c.1966A>T ENSP00000256216.6:p.Lys656Ter
ENST00000414835.6:c.1546A>T ENSP00000411960.2:p.Lys516Ter
ENST00000442060.7:c.*521A>T ENSP00000390208.3:n.*521A>T
ENST00000504811.5:c.2041A>T ENSP00000420914.1:p.Lys681Ter
ENST00000509514.5:c.1180A>T ENSP00000426272.1:p.Lys394Ter
ENST00000509606.1:n.261A>T
ENST00000509951.5:n.309+1397A>T
ENST00000510025.5:c.1894A>T ENSP00000424940.1:p.Lys632Ter
ENST00000513628.5:c.1555A>T ENSP00000425993.1:p.Lys519Ter
ENST00000515235.6:n.3719A>T
ENST00000515320.5:c.1912A>T ENSP00000424613.1:p.Lys638Ter
ENST00000522415.5:n.633A>T
NM_000414.3:c.1966A>T NP_000405.1:p.Lys656Ter
NM_001199291.2:c.2041A>T NP_001186220.1:p.Lys681Ter
NM_001199292.1:c.1912A>T NP_001186221.1:p.Lys638Ter
NM_001292027.1:c.1894A>T NP_001278956.1:p.Lys632Ter
NM_001292028.1:c.1546A>T NP_001278957.1:p.Lys516Ter
NM_000414.4:c.1966A>T MANE Select NP_000405.1:p.Lys656Ter
NM_001199291.3:c.2041A>T NP_001186220.1:p.Lys681Ter
NM_001199292.2:c.1912A>T NP_001186221.1:p.Lys638Ter
NM_001292027.2:c.1894A>T NP_001278956.1:p.Lys632Ter
NM_001292028.2:c.1546A>T NP_001278957.1:p.Lys516Ter
NM_001374497.1:c.1957A>T NP_001361426.1:p.Lys653Ter
NM_001374498.1:c.1894A>T NP_001361427.1:p.Lys632Ter
NM_001374499.1:c.1639A>T NP_001361428.1:p.Lys547Ter
NM_001374500.1:c.1525A>T NP_001361429.1:p.Lys509Ter
NM_001374501.1:c.1555A>T NP_001361430.1:p.Lys519Ter
NM_001374502.1:c.1555A>T NP_001361431.1:p.Lys519Ter
NM_001374503.1:c.1555A>T NP_001361432.1:p.Lys519Ter
NR_164653.1:n.2063A>T
NR_164654.1:n.2331A>T