Canonical Allele Identifier: CA360866175
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478888T>A , CM000667.2:g.119478888T>A GRCh38
NC_000005.9:g.118814583T>A , CM000667.1:g.118814583T>A GRCh37
NC_000005.8:g.118842482T>A NCBI36
NG_008182.1:g.31436T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.489T>A ENSP00000426272.2:p.Asn163Lys
ENST00000518349.6:c.113-17655T>A ENSP00000507185.1:n.113-17655T>A
ENST00000682445.1:c.*370T>A ENSP00000508061.1:n.*370T>A
ENST00000682531.1:n.590T>A
ENST00000682626.1:c.517T>A ENSP00000507857.1:p.Leu173Ile
ENST00000682996.1:c.489T>A ENSP00000507792.1:p.Asn163Lys
ENST00000683265.1:n.582T>A
ENST00000683371.1:c.*619T>A ENSP00000508376.1:n.*619T>A
ENST00000683390.1:n.2179T>A
ENST00000683549.1:n.410T>A
ENST00000683936.1:c.*374T>A ENSP00000507721.1:n.*374T>A
ENST00000683974.1:n.571T>A
ENST00000683996.1:c.78T>A ENSP00000507060.1:p.Asn26Lys
ENST00000684131.1:n.328T>A
ENST00000684160.1:c.*179T>A ENSP00000507821.1:n.*179T>A
ENST00000684214.1:c.489T>A ENSP00000508071.1:p.Asn163Lys
ENST00000414835.7:c.564T>A ENSP00000411960.3:p.Asn188Lys
ENST00000510025.7:c.489T>A MANE Select ENSP00000424940.3:p.Asn163Lys
ENST00000643250.1:c.*361T>A ENSP00000494737.1:n.*361T>A
ENST00000644146.1:c.*67T>A ENSP00000494808.1:n.*67T>A
ENST00000645099.1:c.48T>A ENSP00000496091.1:p.Asn16Lys
ENST00000645702.1:c.78T>A ENSP00000496432.1:p.Asn26Lys
ENST00000645832.1:c.*374T>A ENSP00000494316.1:n.*374T>A
ENST00000646058.1:c.489T>A ENSP00000493579.1:p.Asn163Lys
ENST00000646355.1:c.*495T>A ENSP00000493801.1:n.*495T>A
ENST00000646554.1:c.*467T>A ENSP00000494542.1:n.*467T>A
ENST00000646590.1:c.480T>A ENSP00000494892.1:p.Asn160Lys
ENST00000647335.1:c.*456T>A ENSP00000495180.1:n.*456T>A
ENST00000647342.1:c.*420T>A ENSP00000494992.1:n.*420T>A
ENST00000256216.10:c.489T>A ENSP00000256216.6:p.Asn163Lys
ENST00000414835.6:c.69T>A ENSP00000411960.2:p.Asn23Lys
ENST00000442060.7:c.489T>A ENSP00000390208.3:p.Asn163Lys
ENST00000503168.5:n.478T>A
ENST00000504811.5:c.564T>A ENSP00000420914.1:p.Asn188Lys
ENST00000505181.5:n.192T>A
ENST00000508788.5:n.391T>A
ENST00000509514.5:c.-396T>A ENSP00000426272.1:n.-396T>A
ENST00000510025.5:c.417T>A ENSP00000424940.1:p.Asn139Lys
ENST00000512644.1:n.57T>A
ENST00000512841.5:n.537T>A
ENST00000513628.5:c.78T>A ENSP00000425993.1:p.Asn26Lys
ENST00000515235.6:n.549T>A
ENST00000515320.5:c.435T>A ENSP00000424613.1:p.Asn145Lys
NM_000414.3:c.489T>A NP_000405.1:p.Asn163Lys
NM_001199291.2:c.564T>A NP_001186220.1:p.Asn188Lys
NM_001199292.1:c.435T>A NP_001186221.1:p.Asn145Lys
NM_001292027.1:c.417T>A NP_001278956.1:p.Asn139Lys
NM_001292028.1:c.69T>A NP_001278957.1:p.Asn23Lys
NM_000414.4:c.489T>A MANE Select NP_000405.1:p.Asn163Lys
NM_001199291.3:c.564T>A NP_001186220.1:p.Asn188Lys
NM_001199292.2:c.435T>A NP_001186221.1:p.Asn145Lys
NM_001292027.2:c.417T>A NP_001278956.1:p.Asn139Lys
NM_001292028.2:c.69T>A NP_001278957.1:p.Asn23Lys
NM_001374497.1:c.480T>A NP_001361426.1:p.Asn160Lys
NM_001374498.1:c.489T>A NP_001361427.1:p.Asn163Lys
NM_001374499.1:c.162T>A NP_001361428.1:p.Asn54Lys
NM_001374500.1:c.48T>A NP_001361429.1:p.Asn16Lys
NM_001374501.1:c.78T>A NP_001361430.1:p.Asn26Lys
NM_001374502.1:c.78T>A NP_001361431.1:p.Asn26Lys
NM_001374503.1:c.78T>A NP_001361432.1:p.Asn26Lys
NR_164653.1:n.568T>A
NR_164654.1:n.756T>A