Canonical Allele Identifier: CA1577025548
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478841A= , CM000667.2:g.119478841A= GRCh38
NC_000005.9:g.118814536A= , CM000667.1:g.118814536A= GRCh37
NC_000005.8:g.118842435A= NCBI36
NG_008182.1:g.31389A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.442A= ENSP00000426272.2:p.Met148=
ENST00000518349.6:c.113-17702A= ENSP00000507185.1:n.113-17702A=
ENST00000682445.1:c.*323A= ENSP00000508061.1:n.*323A=
ENST00000682531.1:n.543A=
ENST00000682626.1:c.470A= ENSP00000507857.1:p.Tyr157=
ENST00000682996.1:c.442A= ENSP00000507792.1:p.Met148=
ENST00000683265.1:n.535A=
ENST00000683371.1:c.*572A= ENSP00000508376.1:n.*572A=
ENST00000683390.1:n.2132A=
ENST00000683549.1:n.363A=
ENST00000683936.1:c.*327A= ENSP00000507721.1:n.*327A=
ENST00000683974.1:n.524A=
ENST00000683996.1:c.31A= ENSP00000507060.1:p.Met11=
ENST00000684131.1:n.281A=
ENST00000684160.1:c.*132A= ENSP00000507821.1:n.*132A=
ENST00000684214.1:c.442A= ENSP00000508071.1:p.Met148=
ENST00000414835.7:c.517A= ENSP00000411960.3:p.Met173=
ENST00000510025.7:c.442A= MANE Select ENSP00000424940.3:p.Met148=
ENST00000643250.1:c.*314A= ENSP00000494737.1:n.*314A=
ENST00000644146.1:c.*20A= ENSP00000494808.1:n.*20A=
ENST00000645099.1:c.1A= ENSP00000496091.1:p.Met1=
ENST00000645702.1:c.31A= ENSP00000496432.1:p.Met11=
ENST00000645832.1:c.*327A= ENSP00000494316.1:n.*327A=
ENST00000646058.1:c.442A= ENSP00000493579.1:p.Met148=
ENST00000646355.1:c.*448A= ENSP00000493801.1:n.*448A=
ENST00000646554.1:c.*420A= ENSP00000494542.1:n.*420A=
ENST00000646590.1:c.433A= ENSP00000494892.1:p.Met145=
ENST00000647335.1:c.*409A= ENSP00000495180.1:n.*409A=
ENST00000647342.1:c.*373A= ENSP00000494992.1:n.*373A=
ENST00000256216.10:c.442A= ENSP00000256216.6:p.Met148=
ENST00000414835.6:c.22A= ENSP00000411960.2:p.Met8=
ENST00000442060.7:c.442A= ENSP00000390208.3:p.Met148=
ENST00000503168.5:n.431A=
ENST00000504811.5:c.517A= ENSP00000420914.1:p.Met173=
ENST00000505181.5:n.145A=
ENST00000508788.5:n.344A=
ENST00000509514.5:c.-443A= ENSP00000426272.1:n.-443A=
ENST00000510025.5:c.370A= ENSP00000424940.1:p.Met124=
ENST00000512644.1:n.10A=
ENST00000512841.5:n.490A=
ENST00000513628.5:c.31A= ENSP00000425993.1:p.Met11=
ENST00000515235.6:n.502A=
ENST00000515320.5:c.388A= ENSP00000424613.1:p.Met130=
NM_000414.3:c.442A= NP_000405.1:p.Met148=
NM_001199291.2:c.517A= NP_001186220.1:p.Met173=
NM_001199292.1:c.388A= NP_001186221.1:p.Met130=
NM_001292027.1:c.370A= NP_001278956.1:p.Met124=
NM_001292028.1:c.22A= NP_001278957.1:p.Met8=
NM_000414.4:c.442A= MANE Select NP_000405.1:p.Met148=
NM_001199291.3:c.517A= NP_001186220.1:p.Met173=
NM_001199292.2:c.388A= NP_001186221.1:p.Met130=
NM_001292027.2:c.370A= NP_001278956.1:p.Met124=
NM_001292028.2:c.22A= NP_001278957.1:p.Met8=
NM_001374497.1:c.433A= NP_001361426.1:p.Met145=
NM_001374498.1:c.442A= NP_001361427.1:p.Met148=
NM_001374499.1:c.115A= NP_001361428.1:p.Met39=
NM_001374500.1:c.1A= NP_001361429.1:p.Met1=
NM_001374501.1:c.31A= NP_001361430.1:p.Met11=
NM_001374502.1:c.31A= NP_001361431.1:p.Met11=
NM_001374503.1:c.31A= NP_001361432.1:p.Met11=
NR_164653.1:n.521A=
NR_164654.1:n.709A=