Canonical Allele Identifier: CA1577025602
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478980C= , CM000667.2:g.119478980C= GRCh38
NC_000005.9:g.118814675C= , CM000667.1:g.118814675C= GRCh37
NC_000005.8:g.118842574C= NCBI36
NG_008182.1:g.31528C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.581C= ENSP00000426272.2:p.Pro194=
ENST00000518349.6:c.113-17563C= ENSP00000507185.1:n.113-17563C=
ENST00000682445.1:c.*462C= ENSP00000508061.1:n.*462C=
ENST00000682531.1:n.682C=
ENST00000682626.1:c.*87C= ENSP00000507857.1:n.*87C=
ENST00000682996.1:c.581C= ENSP00000507792.1:p.Pro194=
ENST00000683265.1:n.674C=
ENST00000683371.1:c.*711C= ENSP00000508376.1:n.*711C=
ENST00000683390.1:n.2271C=
ENST00000683549.1:n.502C=
ENST00000683936.1:c.*466C= ENSP00000507721.1:n.*466C=
ENST00000683974.1:n.663C=
ENST00000683996.1:c.170C= ENSP00000507060.1:p.Pro57=
ENST00000684131.1:n.420C=
ENST00000684160.1:c.*271C= ENSP00000507821.1:n.*271C=
ENST00000684214.1:c.581C= ENSP00000508071.1:p.Pro194=
ENST00000414835.7:c.656C= ENSP00000411960.3:p.Pro219=
ENST00000510025.7:c.581C= MANE Select ENSP00000424940.3:p.Pro194=
ENST00000643250.1:c.*453C= ENSP00000494737.1:n.*453C=
ENST00000644146.1:c.*159C= ENSP00000494808.1:n.*159C=
ENST00000645099.1:c.140C= ENSP00000496091.1:p.Pro47=
ENST00000645702.1:c.170C= ENSP00000496432.1:p.Pro57=
ENST00000645832.1:c.*466C= ENSP00000494316.1:n.*466C=
ENST00000646058.1:c.581C= ENSP00000493579.1:p.Pro194=
ENST00000646355.1:c.*587C= ENSP00000493801.1:n.*587C=
ENST00000646554.1:c.*559C= ENSP00000494542.1:n.*559C=
ENST00000647335.1:c.*548C= ENSP00000495180.1:n.*548C=
ENST00000647342.1:c.*512C= ENSP00000494992.1:n.*512C=
ENST00000256216.10:c.581C= ENSP00000256216.6:p.Pro194=
ENST00000414835.6:c.161C= ENSP00000411960.2:p.Pro54=
ENST00000442060.7:c.581C= ENSP00000390208.3:p.Pro194=
ENST00000503168.5:n.570C=
ENST00000504811.5:c.656C= ENSP00000420914.1:p.Pro219=
ENST00000505181.5:n.284C=
ENST00000509514.5:c.-304C= ENSP00000426272.1:n.-304C=
ENST00000510025.5:c.509C= ENSP00000424940.1:p.Pro170=
ENST00000512644.1:n.149C=
ENST00000513628.5:c.170C= ENSP00000425993.1:p.Pro57=
ENST00000515235.6:n.641C=
ENST00000515320.5:c.527C= ENSP00000424613.1:p.Pro176=
NM_000414.3:c.581C= NP_000405.1:p.Pro194=
NM_001199291.2:c.656C= NP_001186220.1:p.Pro219=
NM_001199292.1:c.527C= NP_001186221.1:p.Pro176=
NM_001292027.1:c.509C= NP_001278956.1:p.Pro170=
NM_001292028.1:c.161C= NP_001278957.1:p.Pro54=
NM_000414.4:c.581C= MANE Select NP_000405.1:p.Pro194=
NM_001199291.3:c.656C= NP_001186220.1:p.Pro219=
NM_001199292.2:c.527C= NP_001186221.1:p.Pro176=
NM_001292027.2:c.509C= NP_001278956.1:p.Pro170=
NM_001292028.2:c.161C= NP_001278957.1:p.Pro54=
NM_001374497.1:c.572C= NP_001361426.1:p.Pro191=
NM_001374498.1:c.581C= NP_001361427.1:p.Pro194=
NM_001374499.1:c.254C= NP_001361428.1:p.Pro85=
NM_001374500.1:c.140C= NP_001361429.1:p.Pro47=
NM_001374501.1:c.170C= NP_001361430.1:p.Pro57=
NM_001374502.1:c.170C= NP_001361431.1:p.Pro57=
NM_001374503.1:c.170C= NP_001361432.1:p.Pro57=
NR_164653.1:n.660C=
NR_164654.1:n.848C=