Canonical Allele Identifier: CA1577046961
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119531319G= , CM000667.2:g.119531319G= GRCh38
NC_000005.9:g.118867014G= , CM000667.1:g.118867014G= GRCh37
NC_000005.8:g.118894913G= NCBI36
NG_008182.1:g.83867G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.1839G= ENSP00000426272.2:p.Lys613=
ENST00000518349.6:c.1152G= ENSP00000507185.1:p.Lys384=
ENST00000682445.1:c.*1789G= ENSP00000508061.1:n.*1789G=
ENST00000682531.1:n.3800G=
ENST00000682626.1:c.*1414G= ENSP00000507857.1:n.*1414G=
ENST00000682996.1:c.1836G= ENSP00000507792.1:p.Lys612=
ENST00000683265.1:n.3694G=
ENST00000683335.1:n.3310G=
ENST00000683371.1:c.*2038G= ENSP00000508376.1:n.*2038G=
ENST00000683372.1:n.3918G=
ENST00000683390.1:n.3598G=
ENST00000683476.1:n.750G=
ENST00000683549.1:n.3522G=
ENST00000683936.1:c.*3486G= ENSP00000507721.1:n.*3486G=
ENST00000683974.1:n.3637G=
ENST00000683996.1:c.*1118G= ENSP00000507060.1:n.*1118G=
ENST00000684131.1:n.3440G=
ENST00000684160.1:c.*1598G= ENSP00000507821.1:n.*1598G=
ENST00000684214.1:c.1854+1339G= ENSP00000508071.1:n.1854+1339G=
ENST00000414835.7:c.1983G= ENSP00000411960.3:p.Lys661=
ENST00000510025.7:c.1908G= MANE Select ENSP00000424940.3:p.Lys636=
ENST00000643250.1:c.*1780G= ENSP00000494737.1:n.*1780G=
ENST00000644146.1:c.*3179G= ENSP00000494808.1:n.*3179G=
ENST00000645099.1:c.1467G= ENSP00000496091.1:p.Lys489=
ENST00000645702.1:c.*1311G= ENSP00000496432.1:n.*1311G=
ENST00000645832.1:c.*1793G= ENSP00000494316.1:n.*1793G=
ENST00000646058.1:c.1908G= ENSP00000493579.1:p.Lys636=
ENST00000646355.1:c.*1914G= ENSP00000493801.1:n.*1914G=
ENST00000646554.1:c.*1886G= ENSP00000494542.1:n.*1886G=
ENST00000647335.1:c.*1875G= ENSP00000495180.1:n.*1875G=
ENST00000647342.1:c.*1839G= ENSP00000494992.1:n.*1839G=
ENST00000256216.10:c.1908G= ENSP00000256216.6:p.Lys636=
ENST00000414835.6:c.1488G= ENSP00000411960.2:p.Lys496=
ENST00000442060.7:c.*463G= ENSP00000390208.3:n.*463G=
ENST00000504811.5:c.1983G= ENSP00000420914.1:p.Lys661=
ENST00000509514.5:c.1122G= ENSP00000426272.1:p.Lys374=
ENST00000509606.1:n.203G=
ENST00000509951.5:n.309+1339G=
ENST00000510025.5:c.1836G= ENSP00000424940.1:p.Lys612=
ENST00000513628.5:c.1497G= ENSP00000425993.1:p.Lys499=
ENST00000515235.6:n.3661G=
ENST00000515320.5:c.1854G= ENSP00000424613.1:p.Lys618=
ENST00000522415.5:n.575G=
NM_000414.3:c.1908G= NP_000405.1:p.Lys636=
NM_001199291.2:c.1983G= NP_001186220.1:p.Lys661=
NM_001199292.1:c.1854G= NP_001186221.1:p.Lys618=
NM_001292027.1:c.1836G= NP_001278956.1:p.Lys612=
NM_001292028.1:c.1488G= NP_001278957.1:p.Lys496=
NM_000414.4:c.1908G= MANE Select NP_000405.1:p.Lys636=
NM_001199291.3:c.1983G= NP_001186220.1:p.Lys661=
NM_001199292.2:c.1854G= NP_001186221.1:p.Lys618=
NM_001292027.2:c.1836G= NP_001278956.1:p.Lys612=
NM_001292028.2:c.1488G= NP_001278957.1:p.Lys496=
NM_001374497.1:c.1899G= NP_001361426.1:p.Lys633=
NM_001374498.1:c.1836G= NP_001361427.1:p.Lys612=
NM_001374499.1:c.1581G= NP_001361428.1:p.Lys527=
NM_001374500.1:c.1467G= NP_001361429.1:p.Lys489=
NM_001374501.1:c.1497G= NP_001361430.1:p.Lys499=
NM_001374502.1:c.1497G= NP_001361431.1:p.Lys499=
NM_001374503.1:c.1497G= NP_001361432.1:p.Lys499=
NR_164653.1:n.2005G=
NR_164654.1:n.2273G=