Canonical Allele Identifier: CA360871409
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531387A>C , CM000667.2:g.119531387A>C GRCh38
NC_000005.9:g.118867082A>C , CM000667.1:g.118867082A>C GRCh37
NC_000005.8:g.118894981A>C NCBI36
NG_008182.1:g.83935A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1907A>C ENSP00000426272.2:p.Asn636Thr
ENST00000518349.6:c.1220A>C ENSP00000507185.1:p.Asn407Thr
ENST00000682445.1:c.*1857A>C ENSP00000508061.1:n.*1857A>C
ENST00000682531.1:n.3868A>C
ENST00000682626.1:c.*1482A>C ENSP00000507857.1:n.*1482A>C
ENST00000682996.1:c.1904A>C ENSP00000507792.1:p.Asn635Thr
ENST00000683265.1:n.3762A>C
ENST00000683335.1:n.3378A>C
ENST00000683371.1:c.*2106A>C ENSP00000508376.1:n.*2106A>C
ENST00000683372.1:n.3986A>C
ENST00000683390.1:n.3666A>C
ENST00000683476.1:n.818A>C
ENST00000683549.1:n.3590A>C
ENST00000683936.1:c.*3554A>C ENSP00000507721.1:n.*3554A>C
ENST00000683974.1:n.3705A>C
ENST00000683996.1:c.*1186A>C ENSP00000507060.1:n.*1186A>C
ENST00000684131.1:n.3508A>C
ENST00000684160.1:c.*1666A>C ENSP00000507821.1:n.*1666A>C
ENST00000684214.1:c.1854+1407A>C ENSP00000508071.1:n.1854+1407A>C
ENST00000414835.7:c.2051A>C ENSP00000411960.3:p.Asn684Thr
ENST00000510025.7:c.1976A>C MANE Select ENSP00000424940.3:p.Asn659Thr
ENST00000643250.1:c.*1848A>C ENSP00000494737.1:n.*1848A>C
ENST00000644146.1:c.*3247A>C ENSP00000494808.1:n.*3247A>C
ENST00000645099.1:c.1535A>C ENSP00000496091.1:p.Asn512Thr
ENST00000645702.1:c.*1379A>C ENSP00000496432.1:n.*1379A>C
ENST00000645832.1:c.*1861A>C ENSP00000494316.1:n.*1861A>C
ENST00000646058.1:c.1976A>C ENSP00000493579.1:p.Asn659Thr
ENST00000646355.1:c.*1982A>C ENSP00000493801.1:n.*1982A>C
ENST00000646554.1:c.*1954A>C ENSP00000494542.1:n.*1954A>C
ENST00000647335.1:c.*1943A>C ENSP00000495180.1:n.*1943A>C
ENST00000647342.1:c.*1907A>C ENSP00000494992.1:n.*1907A>C
ENST00000256216.10:c.1976A>C ENSP00000256216.6:p.Asn659Thr
ENST00000414835.6:c.1556A>C ENSP00000411960.2:p.Asn519Thr
ENST00000442060.7:c.*531A>C ENSP00000390208.3:n.*531A>C
ENST00000504811.5:c.2051A>C ENSP00000420914.1:p.Asn684Thr
ENST00000509514.5:c.1190A>C ENSP00000426272.1:p.Asn397Thr
ENST00000509606.1:n.271A>C
ENST00000509951.5:n.309+1407A>C
ENST00000510025.5:c.1904A>C ENSP00000424940.1:p.Asn635Thr
ENST00000513628.5:c.1565A>C ENSP00000425993.1:p.Asn522Thr
ENST00000515235.6:n.3729A>C
ENST00000515320.5:c.1922A>C ENSP00000424613.1:p.Asn641Thr
ENST00000522415.5:n.643A>C
NM_000414.3:c.1976A>C NP_000405.1:p.Asn659Thr
NM_001199291.2:c.2051A>C NP_001186220.1:p.Asn684Thr
NM_001199292.1:c.1922A>C NP_001186221.1:p.Asn641Thr
NM_001292027.1:c.1904A>C NP_001278956.1:p.Asn635Thr
NM_001292028.1:c.1556A>C NP_001278957.1:p.Asn519Thr
NM_000414.4:c.1976A>C MANE Select NP_000405.1:p.Asn659Thr
NM_001199291.3:c.2051A>C NP_001186220.1:p.Asn684Thr
NM_001199292.2:c.1922A>C NP_001186221.1:p.Asn641Thr
NM_001292027.2:c.1904A>C NP_001278956.1:p.Asn635Thr
NM_001292028.2:c.1556A>C NP_001278957.1:p.Asn519Thr
NM_001374497.1:c.1967A>C NP_001361426.1:p.Asn656Thr
NM_001374498.1:c.1904A>C NP_001361427.1:p.Asn635Thr
NM_001374499.1:c.1649A>C NP_001361428.1:p.Asn550Thr
NM_001374500.1:c.1535A>C NP_001361429.1:p.Asn512Thr
NM_001374501.1:c.1565A>C NP_001361430.1:p.Asn522Thr
NM_001374502.1:c.1565A>C NP_001361431.1:p.Asn522Thr
NM_001374503.1:c.1565A>C NP_001361432.1:p.Asn522Thr
NR_164653.1:n.2073A>C
NR_164654.1:n.2341A>C