Canonical Allele Identifier: CA1577025604
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478984T= , CM000667.2:g.119478984T= GRCh38
NC_000005.9:g.118814679T= , CM000667.1:g.118814679T= GRCh37
NC_000005.8:g.118842578T= NCBI36
NG_008182.1:g.31532T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.585T= ENSP00000426272.2:p.Asn195=
ENST00000518349.6:c.113-17559T= ENSP00000507185.1:n.113-17559T=
ENST00000682445.1:c.*466T= ENSP00000508061.1:n.*466T=
ENST00000682531.1:n.686T=
ENST00000682626.1:c.*91T= ENSP00000507857.1:n.*91T=
ENST00000682996.1:c.585T= ENSP00000507792.1:p.Asn195=
ENST00000683265.1:n.678T=
ENST00000683371.1:c.*715T= ENSP00000508376.1:n.*715T=
ENST00000683390.1:n.2275T=
ENST00000683549.1:n.506T=
ENST00000683936.1:c.*470T= ENSP00000507721.1:n.*470T=
ENST00000683974.1:n.667T=
ENST00000683996.1:c.174T= ENSP00000507060.1:p.Asn58=
ENST00000684131.1:n.424T=
ENST00000684160.1:c.*275T= ENSP00000507821.1:n.*275T=
ENST00000684214.1:c.585T= ENSP00000508071.1:p.Asn195=
ENST00000414835.7:c.660T= ENSP00000411960.3:p.Asn220=
ENST00000510025.7:c.585T= MANE Select ENSP00000424940.3:p.Asn195=
ENST00000643250.1:c.*457T= ENSP00000494737.1:n.*457T=
ENST00000644146.1:c.*163T= ENSP00000494808.1:n.*163T=
ENST00000645099.1:c.144T= ENSP00000496091.1:p.Asn48=
ENST00000645702.1:c.174T= ENSP00000496432.1:p.Asn58=
ENST00000645832.1:c.*470T= ENSP00000494316.1:n.*470T=
ENST00000646058.1:c.585T= ENSP00000493579.1:p.Asn195=
ENST00000646355.1:c.*591T= ENSP00000493801.1:n.*591T=
ENST00000646554.1:c.*563T= ENSP00000494542.1:n.*563T=
ENST00000647335.1:c.*552T= ENSP00000495180.1:n.*552T=
ENST00000647342.1:c.*516T= ENSP00000494992.1:n.*516T=
ENST00000256216.10:c.585T= ENSP00000256216.6:p.Asn195=
ENST00000414835.6:c.165T= ENSP00000411960.2:p.Asn55=
ENST00000442060.7:c.585T= ENSP00000390208.3:p.Asn195=
ENST00000503168.5:n.574T=
ENST00000504811.5:c.660T= ENSP00000420914.1:p.Asn220=
ENST00000505181.5:n.288T=
ENST00000509514.5:c.-300T= ENSP00000426272.1:n.-300T=
ENST00000510025.5:c.513T= ENSP00000424940.1:p.Asn171=
ENST00000512644.1:n.153T=
ENST00000513628.5:c.174T= ENSP00000425993.1:p.Asn58=
ENST00000515235.6:n.645T=
ENST00000515320.5:c.531T= ENSP00000424613.1:p.Asn177=
NM_000414.3:c.585T= NP_000405.1:p.Asn195=
NM_001199291.2:c.660T= NP_001186220.1:p.Asn220=
NM_001199292.1:c.531T= NP_001186221.1:p.Asn177=
NM_001292027.1:c.513T= NP_001278956.1:p.Asn171=
NM_001292028.1:c.165T= NP_001278957.1:p.Asn55=
NM_000414.4:c.585T= MANE Select NP_000405.1:p.Asn195=
NM_001199291.3:c.660T= NP_001186220.1:p.Asn220=
NM_001199292.2:c.531T= NP_001186221.1:p.Asn177=
NM_001292027.2:c.513T= NP_001278956.1:p.Asn171=
NM_001292028.2:c.165T= NP_001278957.1:p.Asn55=
NM_001374497.1:c.576T= NP_001361426.1:p.Asn192=
NM_001374498.1:c.585T= NP_001361427.1:p.Asn195=
NM_001374499.1:c.258T= NP_001361428.1:p.Asn86=
NM_001374500.1:c.144T= NP_001361429.1:p.Asn48=
NM_001374501.1:c.174T= NP_001361430.1:p.Asn58=
NM_001374502.1:c.174T= NP_001361431.1:p.Asn58=
NM_001374503.1:c.174T= NP_001361432.1:p.Asn58=
NR_164653.1:n.664T=
NR_164654.1:n.852T=