Canonical Allele Identifier: CA1577025544
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478835A= , CM000667.2:g.119478835A= GRCh38
NC_000005.9:g.118814530A= , CM000667.1:g.118814530A= GRCh37
NC_000005.8:g.118842429A= NCBI36
NG_008182.1:g.31383A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.436A= ENSP00000426272.2:p.Ile146=
ENST00000518349.6:c.113-17708A= ENSP00000507185.1:n.113-17708A=
ENST00000682445.1:c.*317A= ENSP00000508061.1:n.*317A=
ENST00000682531.1:n.537A=
ENST00000682626.1:c.464A= ENSP00000507857.1:p.Asp155=
ENST00000682996.1:c.436A= ENSP00000507792.1:p.Ile146=
ENST00000683265.1:n.529A=
ENST00000683371.1:c.*566A= ENSP00000508376.1:n.*566A=
ENST00000683390.1:n.2126A=
ENST00000683549.1:n.357A=
ENST00000683936.1:c.*321A= ENSP00000507721.1:n.*321A=
ENST00000683974.1:n.518A=
ENST00000683996.1:c.25A= ENSP00000507060.1:p.Ile9=
ENST00000684131.1:n.275A=
ENST00000684160.1:c.*126A= ENSP00000507821.1:n.*126A=
ENST00000684214.1:c.436A= ENSP00000508071.1:p.Ile146=
ENST00000414835.7:c.511A= ENSP00000411960.3:p.Ile171=
ENST00000510025.7:c.436A= MANE Select ENSP00000424940.3:p.Ile146=
ENST00000643250.1:c.*308A= ENSP00000494737.1:n.*308A=
ENST00000644146.1:c.*14A= ENSP00000494808.1:n.*14A=
ENST00000645099.1:c.-6A= ENSP00000496091.1:n.-6A=
ENST00000645702.1:c.25A= ENSP00000496432.1:p.Ile9=
ENST00000645832.1:c.*321A= ENSP00000494316.1:n.*321A=
ENST00000646058.1:c.436A= ENSP00000493579.1:p.Ile146=
ENST00000646355.1:c.*442A= ENSP00000493801.1:n.*442A=
ENST00000646554.1:c.*414A= ENSP00000494542.1:n.*414A=
ENST00000646590.1:c.427A= ENSP00000494892.1:p.Ile143=
ENST00000647335.1:c.*403A= ENSP00000495180.1:n.*403A=
ENST00000647342.1:c.*367A= ENSP00000494992.1:n.*367A=
ENST00000256216.10:c.436A= ENSP00000256216.6:p.Ile146=
ENST00000414835.6:c.16A= ENSP00000411960.2:p.Ile6=
ENST00000442060.7:c.436A= ENSP00000390208.3:p.Ile146=
ENST00000503168.5:n.425A=
ENST00000504811.5:c.511A= ENSP00000420914.1:p.Ile171=
ENST00000505181.5:n.139A=
ENST00000508788.5:n.338A=
ENST00000509514.5:c.-449A= ENSP00000426272.1:n.-449A=
ENST00000510025.5:c.364A= ENSP00000424940.1:p.Ile122=
ENST00000512644.1:n.4A=
ENST00000512841.5:n.484A=
ENST00000513628.5:c.25A= ENSP00000425993.1:p.Ile9=
ENST00000515235.6:n.496A=
ENST00000515320.5:c.382A= ENSP00000424613.1:p.Ile128=
NM_000414.3:c.436A= NP_000405.1:p.Ile146=
NM_001199291.2:c.511A= NP_001186220.1:p.Ile171=
NM_001199292.1:c.382A= NP_001186221.1:p.Ile128=
NM_001292027.1:c.364A= NP_001278956.1:p.Ile122=
NM_001292028.1:c.16A= NP_001278957.1:p.Ile6=
NM_000414.4:c.436A= MANE Select NP_000405.1:p.Ile146=
NM_001199291.3:c.511A= NP_001186220.1:p.Ile171=
NM_001199292.2:c.382A= NP_001186221.1:p.Ile128=
NM_001292027.2:c.364A= NP_001278956.1:p.Ile122=
NM_001292028.2:c.16A= NP_001278957.1:p.Ile6=
NM_001374497.1:c.427A= NP_001361426.1:p.Ile143=
NM_001374498.1:c.436A= NP_001361427.1:p.Ile146=
NM_001374499.1:c.109A= NP_001361428.1:p.Ile37=
NM_001374500.1:c.-6A= NP_001361429.1:n.-6A=
NM_001374501.1:c.25A= NP_001361430.1:p.Ile9=
NM_001374502.1:c.25A= NP_001361431.1:p.Ile9=
NM_001374503.1:c.25A= NP_001361432.1:p.Ile9=
NR_164653.1:n.515A=
NR_164654.1:n.703A=