Canonical Allele Identifier: CA1577025583
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478935C= , CM000667.2:g.119478935C= GRCh38
NC_000005.9:g.118814630C= , CM000667.1:g.118814630C= GRCh37
NC_000005.8:g.118842529C= NCBI36
NG_008182.1:g.31483C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.536C= ENSP00000426272.2:p.Ala179=
ENST00000518349.6:c.113-17608C= ENSP00000507185.1:n.113-17608C=
ENST00000682445.1:c.*417C= ENSP00000508061.1:n.*417C=
ENST00000682531.1:n.637C=
ENST00000682626.1:c.*42C= ENSP00000507857.1:n.*42C=
ENST00000682996.1:c.536C= ENSP00000507792.1:p.Ala179=
ENST00000683265.1:n.629C=
ENST00000683371.1:c.*666C= ENSP00000508376.1:n.*666C=
ENST00000683390.1:n.2226C=
ENST00000683549.1:n.457C=
ENST00000683936.1:c.*421C= ENSP00000507721.1:n.*421C=
ENST00000683974.1:n.618C=
ENST00000683996.1:c.125C= ENSP00000507060.1:p.Ala42=
ENST00000684131.1:n.375C=
ENST00000684160.1:c.*226C= ENSP00000507821.1:n.*226C=
ENST00000684214.1:c.536C= ENSP00000508071.1:p.Ala179=
ENST00000414835.7:c.611C= ENSP00000411960.3:p.Ala204=
ENST00000510025.7:c.536C= MANE Select ENSP00000424940.3:p.Ala179=
ENST00000643250.1:c.*408C= ENSP00000494737.1:n.*408C=
ENST00000644146.1:c.*114C= ENSP00000494808.1:n.*114C=
ENST00000645099.1:c.95C= ENSP00000496091.1:p.Ala32=
ENST00000645702.1:c.125C= ENSP00000496432.1:p.Ala42=
ENST00000645832.1:c.*421C= ENSP00000494316.1:n.*421C=
ENST00000646058.1:c.536C= ENSP00000493579.1:p.Ala179=
ENST00000646355.1:c.*542C= ENSP00000493801.1:n.*542C=
ENST00000646554.1:c.*514C= ENSP00000494542.1:n.*514C=
ENST00000647335.1:c.*503C= ENSP00000495180.1:n.*503C=
ENST00000647342.1:c.*467C= ENSP00000494992.1:n.*467C=
ENST00000256216.10:c.536C= ENSP00000256216.6:p.Ala179=
ENST00000414835.6:c.116C= ENSP00000411960.2:p.Ala39=
ENST00000442060.7:c.536C= ENSP00000390208.3:p.Ala179=
ENST00000503168.5:n.525C=
ENST00000504811.5:c.611C= ENSP00000420914.1:p.Ala204=
ENST00000505181.5:n.239C=
ENST00000508788.5:n.438C=
ENST00000509514.5:c.-349C= ENSP00000426272.1:n.-349C=
ENST00000510025.5:c.464C= ENSP00000424940.1:p.Ala155=
ENST00000512644.1:n.104C=
ENST00000512841.5:n.584C=
ENST00000513628.5:c.125C= ENSP00000425993.1:p.Ala42=
ENST00000515235.6:n.596C=
ENST00000515320.5:c.482C= ENSP00000424613.1:p.Ala161=
NM_000414.3:c.536C= NP_000405.1:p.Ala179=
NM_001199291.2:c.611C= NP_001186220.1:p.Ala204=
NM_001199292.1:c.482C= NP_001186221.1:p.Ala161=
NM_001292027.1:c.464C= NP_001278956.1:p.Ala155=
NM_001292028.1:c.116C= NP_001278957.1:p.Ala39=
NM_000414.4:c.536C= MANE Select NP_000405.1:p.Ala179=
NM_001199291.3:c.611C= NP_001186220.1:p.Ala204=
NM_001199292.2:c.482C= NP_001186221.1:p.Ala161=
NM_001292027.2:c.464C= NP_001278956.1:p.Ala155=
NM_001292028.2:c.116C= NP_001278957.1:p.Ala39=
NM_001374497.1:c.527C= NP_001361426.1:p.Ala176=
NM_001374498.1:c.536C= NP_001361427.1:p.Ala179=
NM_001374499.1:c.209C= NP_001361428.1:p.Ala70=
NM_001374500.1:c.95C= NP_001361429.1:p.Ala32=
NM_001374501.1:c.125C= NP_001361430.1:p.Ala42=
NM_001374502.1:c.125C= NP_001361431.1:p.Ala42=
NM_001374503.1:c.125C= NP_001361432.1:p.Ala42=
NR_164653.1:n.615C=
NR_164654.1:n.803C=