Canonical Allele Identifier: CA360866091
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478850T>C , CM000667.2:g.119478850T>C GRCh38
NC_000005.9:g.118814545T>C , CM000667.1:g.118814545T>C GRCh37
NC_000005.8:g.118842444T>C NCBI36
NG_008182.1:g.31398T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.451T>C ENSP00000426272.2:p.Ser151Pro
ENST00000518349.6:c.113-17693T>C ENSP00000507185.1:n.113-17693T>C
ENST00000682445.1:c.*332T>C ENSP00000508061.1:n.*332T>C
ENST00000682531.1:n.552T>C
ENST00000682626.1:c.479T>C ENSP00000507857.1:p.Ile160Thr
ENST00000682996.1:c.451T>C ENSP00000507792.1:p.Ser151Pro
ENST00000683265.1:n.544T>C
ENST00000683371.1:c.*581T>C ENSP00000508376.1:n.*581T>C
ENST00000683390.1:n.2141T>C
ENST00000683549.1:n.372T>C
ENST00000683936.1:c.*336T>C ENSP00000507721.1:n.*336T>C
ENST00000683974.1:n.533T>C
ENST00000683996.1:c.40T>C ENSP00000507060.1:p.Ser14Pro
ENST00000684131.1:n.290T>C
ENST00000684160.1:c.*141T>C ENSP00000507821.1:n.*141T>C
ENST00000684214.1:c.451T>C ENSP00000508071.1:p.Ser151Pro
ENST00000414835.7:c.526T>C ENSP00000411960.3:p.Ser176Pro
ENST00000510025.7:c.451T>C MANE Select ENSP00000424940.3:p.Ser151Pro
ENST00000643250.1:c.*323T>C ENSP00000494737.1:n.*323T>C
ENST00000644146.1:c.*29T>C ENSP00000494808.1:n.*29T>C
ENST00000645099.1:c.10T>C ENSP00000496091.1:p.Ser4Pro
ENST00000645702.1:c.40T>C ENSP00000496432.1:p.Ser14Pro
ENST00000645832.1:c.*336T>C ENSP00000494316.1:n.*336T>C
ENST00000646058.1:c.451T>C ENSP00000493579.1:p.Ser151Pro
ENST00000646355.1:c.*457T>C ENSP00000493801.1:n.*457T>C
ENST00000646554.1:c.*429T>C ENSP00000494542.1:n.*429T>C
ENST00000646590.1:c.442T>C ENSP00000494892.1:p.Ser148Pro
ENST00000647335.1:c.*418T>C ENSP00000495180.1:n.*418T>C
ENST00000647342.1:c.*382T>C ENSP00000494992.1:n.*382T>C
ENST00000256216.10:c.451T>C ENSP00000256216.6:p.Ser151Pro
ENST00000414835.6:c.31T>C ENSP00000411960.2:p.Ser11Pro
ENST00000442060.7:c.451T>C ENSP00000390208.3:p.Ser151Pro
ENST00000503168.5:n.440T>C
ENST00000504811.5:c.526T>C ENSP00000420914.1:p.Ser176Pro
ENST00000505181.5:n.154T>C
ENST00000508788.5:n.353T>C
ENST00000509514.5:c.-434T>C ENSP00000426272.1:n.-434T>C
ENST00000510025.5:c.379T>C ENSP00000424940.1:p.Ser127Pro
ENST00000512644.1:n.19T>C
ENST00000512841.5:n.499T>C
ENST00000513628.5:c.40T>C ENSP00000425993.1:p.Ser14Pro
ENST00000515235.6:n.511T>C
ENST00000515320.5:c.397T>C ENSP00000424613.1:p.Ser133Pro
NM_000414.3:c.451T>C NP_000405.1:p.Ser151Pro
NM_001199291.2:c.526T>C NP_001186220.1:p.Ser176Pro
NM_001199292.1:c.397T>C NP_001186221.1:p.Ser133Pro
NM_001292027.1:c.379T>C NP_001278956.1:p.Ser127Pro
NM_001292028.1:c.31T>C NP_001278957.1:p.Ser11Pro
NM_000414.4:c.451T>C MANE Select NP_000405.1:p.Ser151Pro
NM_001199291.3:c.526T>C NP_001186220.1:p.Ser176Pro
NM_001199292.2:c.397T>C NP_001186221.1:p.Ser133Pro
NM_001292027.2:c.379T>C NP_001278956.1:p.Ser127Pro
NM_001292028.2:c.31T>C NP_001278957.1:p.Ser11Pro
NM_001374497.1:c.442T>C NP_001361426.1:p.Ser148Pro
NM_001374498.1:c.451T>C NP_001361427.1:p.Ser151Pro
NM_001374499.1:c.124T>C NP_001361428.1:p.Ser42Pro
NM_001374500.1:c.10T>C NP_001361429.1:p.Ser4Pro
NM_001374501.1:c.40T>C NP_001361430.1:p.Ser14Pro
NM_001374502.1:c.40T>C NP_001361431.1:p.Ser14Pro
NM_001374503.1:c.40T>C NP_001361432.1:p.Ser14Pro
NR_164653.1:n.530T>C
NR_164654.1:n.718T>C