Canonical Allele Identifier: CA360866206
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478901A>C , CM000667.2:g.119478901A>C GRCh38
NC_000005.9:g.118814596A>C , CM000667.1:g.118814596A>C GRCh37
NC_000005.8:g.118842495A>C NCBI36
NG_008182.1:g.31449A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.502A>C ENSP00000426272.2:p.Lys168Gln
ENST00000518349.6:c.113-17642A>C ENSP00000507185.1:n.113-17642A>C
ENST00000682445.1:c.*383A>C ENSP00000508061.1:n.*383A>C
ENST00000682531.1:n.603A>C
ENST00000682626.1:c.*8A>C ENSP00000507857.1:n.*8A>C
ENST00000682996.1:c.502A>C ENSP00000507792.1:p.Lys168Gln
ENST00000683265.1:n.595A>C
ENST00000683371.1:c.*632A>C ENSP00000508376.1:n.*632A>C
ENST00000683390.1:n.2192A>C
ENST00000683549.1:n.423A>C
ENST00000683936.1:c.*387A>C ENSP00000507721.1:n.*387A>C
ENST00000683974.1:n.584A>C
ENST00000683996.1:c.91A>C ENSP00000507060.1:p.Lys31Gln
ENST00000684131.1:n.341A>C
ENST00000684160.1:c.*192A>C ENSP00000507821.1:n.*192A>C
ENST00000684214.1:c.502A>C ENSP00000508071.1:p.Lys168Gln
ENST00000414835.7:c.577A>C ENSP00000411960.3:p.Lys193Gln
ENST00000510025.7:c.502A>C MANE Select ENSP00000424940.3:p.Lys168Gln
ENST00000643250.1:c.*374A>C ENSP00000494737.1:n.*374A>C
ENST00000644146.1:c.*80A>C ENSP00000494808.1:n.*80A>C
ENST00000645099.1:c.61A>C ENSP00000496091.1:p.Lys21Gln
ENST00000645702.1:c.91A>C ENSP00000496432.1:p.Lys31Gln
ENST00000645832.1:c.*387A>C ENSP00000494316.1:n.*387A>C
ENST00000646058.1:c.502A>C ENSP00000493579.1:p.Lys168Gln
ENST00000646355.1:c.*508A>C ENSP00000493801.1:n.*508A>C
ENST00000646554.1:c.*480A>C ENSP00000494542.1:n.*480A>C
ENST00000646590.1:c.493A>C ENSP00000494892.1:p.Lys165Gln
ENST00000647335.1:c.*469A>C ENSP00000495180.1:n.*469A>C
ENST00000647342.1:c.*433A>C ENSP00000494992.1:n.*433A>C
ENST00000256216.10:c.502A>C ENSP00000256216.6:p.Lys168Gln
ENST00000414835.6:c.82A>C ENSP00000411960.2:p.Lys28Gln
ENST00000442060.7:c.502A>C ENSP00000390208.3:p.Lys168Gln
ENST00000503168.5:n.491A>C
ENST00000504811.5:c.577A>C ENSP00000420914.1:p.Lys193Gln
ENST00000505181.5:n.205A>C
ENST00000508788.5:n.404A>C
ENST00000509514.5:c.-383A>C ENSP00000426272.1:n.-383A>C
ENST00000510025.5:c.430A>C ENSP00000424940.1:p.Lys144Gln
ENST00000512644.1:n.70A>C
ENST00000512841.5:n.550A>C
ENST00000513628.5:c.91A>C ENSP00000425993.1:p.Lys31Gln
ENST00000515235.6:n.562A>C
ENST00000515320.5:c.448A>C ENSP00000424613.1:p.Lys150Gln
NM_000414.3:c.502A>C NP_000405.1:p.Lys168Gln
NM_001199291.2:c.577A>C NP_001186220.1:p.Lys193Gln
NM_001199292.1:c.448A>C NP_001186221.1:p.Lys150Gln
NM_001292027.1:c.430A>C NP_001278956.1:p.Lys144Gln
NM_001292028.1:c.82A>C NP_001278957.1:p.Lys28Gln
NM_000414.4:c.502A>C MANE Select NP_000405.1:p.Lys168Gln
NM_001199291.3:c.577A>C NP_001186220.1:p.Lys193Gln
NM_001199292.2:c.448A>C NP_001186221.1:p.Lys150Gln
NM_001292027.2:c.430A>C NP_001278956.1:p.Lys144Gln
NM_001292028.2:c.82A>C NP_001278957.1:p.Lys28Gln
NM_001374497.1:c.493A>C NP_001361426.1:p.Lys165Gln
NM_001374498.1:c.502A>C NP_001361427.1:p.Lys168Gln
NM_001374499.1:c.175A>C NP_001361428.1:p.Lys59Gln
NM_001374500.1:c.61A>C NP_001361429.1:p.Lys21Gln
NM_001374501.1:c.91A>C NP_001361430.1:p.Lys31Gln
NM_001374502.1:c.91A>C NP_001361431.1:p.Lys31Gln
NM_001374503.1:c.91A>C NP_001361432.1:p.Lys31Gln
NR_164653.1:n.581A>C
NR_164654.1:n.769A>C