Canonical Allele Identifier: CA1577025611
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478999G= , CM000667.2:g.119478999G= GRCh38
NC_000005.9:g.118814694G= , CM000667.1:g.118814694G= GRCh37
NC_000005.8:g.118842593G= NCBI36
NG_008182.1:g.31547G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.600G= ENSP00000426272.2:p.Met200=
ENST00000518349.6:c.113-17544G= ENSP00000507185.1:n.113-17544G=
ENST00000682445.1:c.*481G= ENSP00000508061.1:n.*481G=
ENST00000682531.1:n.701G=
ENST00000682626.1:c.*106G= ENSP00000507857.1:n.*106G=
ENST00000682996.1:c.600G= ENSP00000507792.1:p.Met200=
ENST00000683265.1:n.693G=
ENST00000683371.1:c.*730G= ENSP00000508376.1:n.*730G=
ENST00000683390.1:n.2290G=
ENST00000683549.1:n.521G=
ENST00000683936.1:c.*485G= ENSP00000507721.1:n.*485G=
ENST00000683974.1:n.682G=
ENST00000683996.1:c.189G= ENSP00000507060.1:p.Met63=
ENST00000684131.1:n.439G=
ENST00000684160.1:c.*290G= ENSP00000507821.1:n.*290G=
ENST00000684214.1:c.600G= ENSP00000508071.1:p.Met200=
ENST00000414835.7:c.675G= ENSP00000411960.3:p.Met225=
ENST00000510025.7:c.600G= MANE Select ENSP00000424940.3:p.Met200=
ENST00000643250.1:c.*472G= ENSP00000494737.1:n.*472G=
ENST00000644146.1:c.*178G= ENSP00000494808.1:n.*178G=
ENST00000645099.1:c.159G= ENSP00000496091.1:p.Met53=
ENST00000645702.1:c.189G= ENSP00000496432.1:p.Met63=
ENST00000645832.1:c.*485G= ENSP00000494316.1:n.*485G=
ENST00000646058.1:c.600G= ENSP00000493579.1:p.Met200=
ENST00000646355.1:c.*606G= ENSP00000493801.1:n.*606G=
ENST00000646554.1:c.*578G= ENSP00000494542.1:n.*578G=
ENST00000647335.1:c.*567G= ENSP00000495180.1:n.*567G=
ENST00000647342.1:c.*531G= ENSP00000494992.1:n.*531G=
ENST00000256216.10:c.600G= ENSP00000256216.6:p.Met200=
ENST00000414835.6:c.180G= ENSP00000411960.2:p.Met60=
ENST00000442060.7:c.600G= ENSP00000390208.3:p.Met200=
ENST00000503168.5:n.589G=
ENST00000504811.5:c.675G= ENSP00000420914.1:p.Met225=
ENST00000505181.5:n.303G=
ENST00000509514.5:c.-285G= ENSP00000426272.1:n.-285G=
ENST00000510025.5:c.528G= ENSP00000424940.1:p.Met176=
ENST00000512644.1:n.168G=
ENST00000513628.5:c.189G= ENSP00000425993.1:p.Met63=
ENST00000515235.6:n.660G=
ENST00000515320.5:c.546G= ENSP00000424613.1:p.Met182=
NM_000414.3:c.600G= NP_000405.1:p.Met200=
NM_001199291.2:c.675G= NP_001186220.1:p.Met225=
NM_001199292.1:c.546G= NP_001186221.1:p.Met182=
NM_001292027.1:c.528G= NP_001278956.1:p.Met176=
NM_001292028.1:c.180G= NP_001278957.1:p.Met60=
NM_000414.4:c.600G= MANE Select NP_000405.1:p.Met200=
NM_001199291.3:c.675G= NP_001186220.1:p.Met225=
NM_001199292.2:c.546G= NP_001186221.1:p.Met182=
NM_001292027.2:c.528G= NP_001278956.1:p.Met176=
NM_001292028.2:c.180G= NP_001278957.1:p.Met60=
NM_001374497.1:c.591G= NP_001361426.1:p.Met197=
NM_001374498.1:c.600G= NP_001361427.1:p.Met200=
NM_001374499.1:c.273G= NP_001361428.1:p.Met91=
NM_001374500.1:c.159G= NP_001361429.1:p.Met53=
NM_001374501.1:c.189G= NP_001361430.1:p.Met63=
NM_001374502.1:c.189G= NP_001361431.1:p.Met63=
NM_001374503.1:c.189G= NP_001361432.1:p.Met63=
NR_164653.1:n.679G=
NR_164654.1:n.867G=