Canonical Allele Identifier: CA1577025591
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478956A= , CM000667.2:g.119478956A= GRCh38
NC_000005.9:g.118814651A= , CM000667.1:g.118814651A= GRCh37
NC_000005.8:g.118842550A= NCBI36
NG_008182.1:g.31504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.557A= ENSP00000426272.2:p.Asn186=
ENST00000518349.6:c.113-17587A= ENSP00000507185.1:n.113-17587A=
ENST00000682445.1:c.*438A= ENSP00000508061.1:n.*438A=
ENST00000682531.1:n.658A=
ENST00000682626.1:c.*63A= ENSP00000507857.1:n.*63A=
ENST00000682996.1:c.557A= ENSP00000507792.1:p.Asn186=
ENST00000683265.1:n.650A=
ENST00000683371.1:c.*687A= ENSP00000508376.1:n.*687A=
ENST00000683390.1:n.2247A=
ENST00000683549.1:n.478A=
ENST00000683936.1:c.*442A= ENSP00000507721.1:n.*442A=
ENST00000683974.1:n.639A=
ENST00000683996.1:c.146A= ENSP00000507060.1:p.Asn49=
ENST00000684131.1:n.396A=
ENST00000684160.1:c.*247A= ENSP00000507821.1:n.*247A=
ENST00000684214.1:c.557A= ENSP00000508071.1:p.Asn186=
ENST00000414835.7:c.632A= ENSP00000411960.3:p.Asn211=
ENST00000510025.7:c.557A= MANE Select ENSP00000424940.3:p.Asn186=
ENST00000643250.1:c.*429A= ENSP00000494737.1:n.*429A=
ENST00000644146.1:c.*135A= ENSP00000494808.1:n.*135A=
ENST00000645099.1:c.116A= ENSP00000496091.1:p.Asn39=
ENST00000645702.1:c.146A= ENSP00000496432.1:p.Asn49=
ENST00000645832.1:c.*442A= ENSP00000494316.1:n.*442A=
ENST00000646058.1:c.557A= ENSP00000493579.1:p.Asn186=
ENST00000646355.1:c.*563A= ENSP00000493801.1:n.*563A=
ENST00000646554.1:c.*535A= ENSP00000494542.1:n.*535A=
ENST00000647335.1:c.*524A= ENSP00000495180.1:n.*524A=
ENST00000647342.1:c.*488A= ENSP00000494992.1:n.*488A=
ENST00000256216.10:c.557A= ENSP00000256216.6:p.Asn186=
ENST00000414835.6:c.137A= ENSP00000411960.2:p.Asn46=
ENST00000442060.7:c.557A= ENSP00000390208.3:p.Asn186=
ENST00000503168.5:n.546A=
ENST00000504811.5:c.632A= ENSP00000420914.1:p.Asn211=
ENST00000505181.5:n.260A=
ENST00000509514.5:c.-328A= ENSP00000426272.1:n.-328A=
ENST00000510025.5:c.485A= ENSP00000424940.1:p.Asn162=
ENST00000512644.1:n.125A=
ENST00000513628.5:c.146A= ENSP00000425993.1:p.Asn49=
ENST00000515235.6:n.617A=
ENST00000515320.5:c.503A= ENSP00000424613.1:p.Asn168=
NM_000414.3:c.557A= NP_000405.1:p.Asn186=
NM_001199291.2:c.632A= NP_001186220.1:p.Asn211=
NM_001199292.1:c.503A= NP_001186221.1:p.Asn168=
NM_001292027.1:c.485A= NP_001278956.1:p.Asn162=
NM_001292028.1:c.137A= NP_001278957.1:p.Asn46=
NM_000414.4:c.557A= MANE Select NP_000405.1:p.Asn186=
NM_001199291.3:c.632A= NP_001186220.1:p.Asn211=
NM_001199292.2:c.503A= NP_001186221.1:p.Asn168=
NM_001292027.2:c.485A= NP_001278956.1:p.Asn162=
NM_001292028.2:c.137A= NP_001278957.1:p.Asn46=
NM_001374497.1:c.548A= NP_001361426.1:p.Asn183=
NM_001374498.1:c.557A= NP_001361427.1:p.Asn186=
NM_001374499.1:c.230A= NP_001361428.1:p.Asn77=
NM_001374500.1:c.116A= NP_001361429.1:p.Asn39=
NM_001374501.1:c.146A= NP_001361430.1:p.Asn49=
NM_001374502.1:c.146A= NP_001361431.1:p.Asn49=
NM_001374503.1:c.146A= NP_001361432.1:p.Asn49=
NR_164653.1:n.636A=
NR_164654.1:n.824A=