Canonical Allele Identifier: CA1577025549
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478843G= , CM000667.2:g.119478843G= GRCh38
NC_000005.9:g.118814538G= , CM000667.1:g.118814538G= GRCh37
NC_000005.8:g.118842437G= NCBI36
NG_008182.1:g.31391G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.444G= ENSP00000426272.2:p.Met148=
ENST00000518349.6:c.113-17700G= ENSP00000507185.1:n.113-17700G=
ENST00000682445.1:c.*325G= ENSP00000508061.1:n.*325G=
ENST00000682531.1:n.545G=
ENST00000682626.1:c.472G= ENSP00000507857.1:p.Asp158=
ENST00000682996.1:c.444G= ENSP00000507792.1:p.Met148=
ENST00000683265.1:n.537G=
ENST00000683371.1:c.*574G= ENSP00000508376.1:n.*574G=
ENST00000683390.1:n.2134G=
ENST00000683549.1:n.365G=
ENST00000683936.1:c.*329G= ENSP00000507721.1:n.*329G=
ENST00000683974.1:n.526G=
ENST00000683996.1:c.33G= ENSP00000507060.1:p.Met11=
ENST00000684131.1:n.283G=
ENST00000684160.1:c.*134G= ENSP00000507821.1:n.*134G=
ENST00000684214.1:c.444G= ENSP00000508071.1:p.Met148=
ENST00000414835.7:c.519G= ENSP00000411960.3:p.Met173=
ENST00000510025.7:c.444G= MANE Select ENSP00000424940.3:p.Met148=
ENST00000643250.1:c.*316G= ENSP00000494737.1:n.*316G=
ENST00000644146.1:c.*22G= ENSP00000494808.1:n.*22G=
ENST00000645099.1:c.3G= ENSP00000496091.1:p.Met1=
ENST00000645702.1:c.33G= ENSP00000496432.1:p.Met11=
ENST00000645832.1:c.*329G= ENSP00000494316.1:n.*329G=
ENST00000646058.1:c.444G= ENSP00000493579.1:p.Met148=
ENST00000646355.1:c.*450G= ENSP00000493801.1:n.*450G=
ENST00000646554.1:c.*422G= ENSP00000494542.1:n.*422G=
ENST00000646590.1:c.435G= ENSP00000494892.1:p.Met145=
ENST00000647335.1:c.*411G= ENSP00000495180.1:n.*411G=
ENST00000647342.1:c.*375G= ENSP00000494992.1:n.*375G=
ENST00000256216.10:c.444G= ENSP00000256216.6:p.Met148=
ENST00000414835.6:c.24G= ENSP00000411960.2:p.Met8=
ENST00000442060.7:c.444G= ENSP00000390208.3:p.Met148=
ENST00000503168.5:n.433G=
ENST00000504811.5:c.519G= ENSP00000420914.1:p.Met173=
ENST00000505181.5:n.147G=
ENST00000508788.5:n.346G=
ENST00000509514.5:c.-441G= ENSP00000426272.1:n.-441G=
ENST00000510025.5:c.372G= ENSP00000424940.1:p.Met124=
ENST00000512644.1:n.12G=
ENST00000512841.5:n.492G=
ENST00000513628.5:c.33G= ENSP00000425993.1:p.Met11=
ENST00000515235.6:n.504G=
ENST00000515320.5:c.390G= ENSP00000424613.1:p.Met130=
NM_000414.3:c.444G= NP_000405.1:p.Met148=
NM_001199291.2:c.519G= NP_001186220.1:p.Met173=
NM_001199292.1:c.390G= NP_001186221.1:p.Met130=
NM_001292027.1:c.372G= NP_001278956.1:p.Met124=
NM_001292028.1:c.24G= NP_001278957.1:p.Met8=
NM_000414.4:c.444G= MANE Select NP_000405.1:p.Met148=
NM_001199291.3:c.519G= NP_001186220.1:p.Met173=
NM_001199292.2:c.390G= NP_001186221.1:p.Met130=
NM_001292027.2:c.372G= NP_001278956.1:p.Met124=
NM_001292028.2:c.24G= NP_001278957.1:p.Met8=
NM_001374497.1:c.435G= NP_001361426.1:p.Met145=
NM_001374498.1:c.444G= NP_001361427.1:p.Met148=
NM_001374499.1:c.117G= NP_001361428.1:p.Met39=
NM_001374500.1:c.3G= NP_001361429.1:p.Met1=
NM_001374501.1:c.33G= NP_001361430.1:p.Met11=
NM_001374502.1:c.33G= NP_001361431.1:p.Met11=
NM_001374503.1:c.33G= NP_001361432.1:p.Met11=
NR_164653.1:n.523G=
NR_164654.1:n.711G=