Canonical Allele Identifier: CA1577025563
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478881A= , CM000667.2:g.119478881A= GRCh38
NC_000005.9:g.118814576A= , CM000667.1:g.118814576A= GRCh37
NC_000005.8:g.118842475A= NCBI36
NG_008182.1:g.31429A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.482A= ENSP00000426272.2:p.Gln161=
ENST00000518349.6:c.113-17662A= ENSP00000507185.1:n.113-17662A=
ENST00000682445.1:c.*363A= ENSP00000508061.1:n.*363A=
ENST00000682531.1:n.583A=
ENST00000682626.1:c.510A= ENSP00000507857.1:p.Pro170=
ENST00000682996.1:c.482A= ENSP00000507792.1:p.Gln161=
ENST00000683265.1:n.575A=
ENST00000683371.1:c.*612A= ENSP00000508376.1:n.*612A=
ENST00000683390.1:n.2172A=
ENST00000683549.1:n.403A=
ENST00000683936.1:c.*367A= ENSP00000507721.1:n.*367A=
ENST00000683974.1:n.564A=
ENST00000683996.1:c.71A= ENSP00000507060.1:p.Gln24=
ENST00000684131.1:n.321A=
ENST00000684160.1:c.*172A= ENSP00000507821.1:n.*172A=
ENST00000684214.1:c.482A= ENSP00000508071.1:p.Gln161=
ENST00000414835.7:c.557A= ENSP00000411960.3:p.Gln186=
ENST00000510025.7:c.482A= MANE Select ENSP00000424940.3:p.Gln161=
ENST00000643250.1:c.*354A= ENSP00000494737.1:n.*354A=
ENST00000644146.1:c.*60A= ENSP00000494808.1:n.*60A=
ENST00000645099.1:c.41A= ENSP00000496091.1:p.Gln14=
ENST00000645702.1:c.71A= ENSP00000496432.1:p.Gln24=
ENST00000645832.1:c.*367A= ENSP00000494316.1:n.*367A=
ENST00000646058.1:c.482A= ENSP00000493579.1:p.Gln161=
ENST00000646355.1:c.*488A= ENSP00000493801.1:n.*488A=
ENST00000646554.1:c.*460A= ENSP00000494542.1:n.*460A=
ENST00000646590.1:c.473A= ENSP00000494892.1:p.Gln158=
ENST00000647335.1:c.*449A= ENSP00000495180.1:n.*449A=
ENST00000647342.1:c.*413A= ENSP00000494992.1:n.*413A=
ENST00000256216.10:c.482A= ENSP00000256216.6:p.Gln161=
ENST00000414835.6:c.62A= ENSP00000411960.2:p.Gln21=
ENST00000442060.7:c.482A= ENSP00000390208.3:p.Gln161=
ENST00000503168.5:n.471A=
ENST00000504811.5:c.557A= ENSP00000420914.1:p.Gln186=
ENST00000505181.5:n.185A=
ENST00000508788.5:n.384A=
ENST00000509514.5:c.-403A= ENSP00000426272.1:n.-403A=
ENST00000510025.5:c.410A= ENSP00000424940.1:p.Gln137=
ENST00000512644.1:n.50A=
ENST00000512841.5:n.530A=
ENST00000513628.5:c.71A= ENSP00000425993.1:p.Gln24=
ENST00000515235.6:n.542A=
ENST00000515320.5:c.428A= ENSP00000424613.1:p.Gln143=
NM_000414.3:c.482A= NP_000405.1:p.Gln161=
NM_001199291.2:c.557A= NP_001186220.1:p.Gln186=
NM_001199292.1:c.428A= NP_001186221.1:p.Gln143=
NM_001292027.1:c.410A= NP_001278956.1:p.Gln137=
NM_001292028.1:c.62A= NP_001278957.1:p.Gln21=
NM_000414.4:c.482A= MANE Select NP_000405.1:p.Gln161=
NM_001199291.3:c.557A= NP_001186220.1:p.Gln186=
NM_001199292.2:c.428A= NP_001186221.1:p.Gln143=
NM_001292027.2:c.410A= NP_001278956.1:p.Gln137=
NM_001292028.2:c.62A= NP_001278957.1:p.Gln21=
NM_001374497.1:c.473A= NP_001361426.1:p.Gln158=
NM_001374498.1:c.482A= NP_001361427.1:p.Gln161=
NM_001374499.1:c.155A= NP_001361428.1:p.Gln52=
NM_001374500.1:c.41A= NP_001361429.1:p.Gln14=
NM_001374501.1:c.71A= NP_001361430.1:p.Gln24=
NM_001374502.1:c.71A= NP_001361431.1:p.Gln24=
NM_001374503.1:c.71A= NP_001361432.1:p.Gln24=
NR_164653.1:n.561A=
NR_164654.1:n.749A=