Canonical Allele Identifier: CA1577006926
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452633G= , CM000667.2:g.119452633G= GRCh38
NC_000005.9:g.118788328G= , CM000667.1:g.118788328G= GRCh37
NC_000005.8:g.118816227G= NCBI36
NG_008182.1:g.5181G=

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.58G= ENSP00000426272.2:p.Gly20=
ENST00000512841.6:n.99G=
ENST00000518349.6:c.58G= ENSP00000507185.1:p.Gly20=
ENST00000682445.1:c.58G= ENSP00000508061.1:p.Gly20=
ENST00000682996.1:c.58G= ENSP00000507792.1:p.Gly20=
ENST00000683371.1:c.58G= ENSP00000508376.1:p.Gly20=
ENST00000683390.1:n.106G=
ENST00000683936.1:c.58G= ENSP00000507721.1:p.Gly20=
ENST00000683974.1:n.140G=
ENST00000684214.1:c.58G= ENSP00000508071.1:p.Gly20=
ENST00000414835.7:c.-121G= ENSP00000411960.3:n.-121G=
ENST00000510025.7:c.58G= MANE Select ENSP00000424940.3:p.Gly20=
ENST00000644146.1:c.58G= ENSP00000494808.1:p.Gly20=
ENST00000645832.1:c.58G= ENSP00000494316.1:p.Gly20=
ENST00000646058.1:c.58G= ENSP00000493579.1:p.Gly20=
ENST00000646590.1:c.58G= ENSP00000494892.1:p.Gly20=
ENST00000256216.10:c.58G= ENSP00000256216.6:p.Gly20=
ENST00000442060.7:c.58G= ENSP00000390208.3:p.Gly20=
ENST00000504811.5:c.-121G= ENSP00000420914.1:n.-121G=
ENST00000510025.5:c.-80G= ENSP00000424940.1:n.-80G=
ENST00000511186.5:n.161G=
ENST00000515235.6:n.118G=
ENST00000515320.5:c.58G= ENSP00000424613.1:p.Val20=
ENST00000519184.5:n.69G=
NM_000414.3:c.58G= NP_000405.1:p.Gly20=
NM_001199291.2:c.-121G= NP_001186220.1:n.-121G=
NM_001199292.1:c.58G= NP_001186221.1:p.Val20=
NM_001292027.1:c.-80G= NP_001278956.1:n.-80G=
NM_001292028.1:c.-542G= NP_001278957.1:n.-542G=
NM_000414.4:c.58G= MANE Select NP_000405.1:p.Gly20=
NM_001199291.3:c.-121G= NP_001186220.1:n.-121G=
NM_001199292.2:c.58G= NP_001186221.1:p.Val20=
NM_001292027.2:c.-80G= NP_001278956.1:n.-80G=
NM_001292028.2:c.-542G= NP_001278957.1:n.-542G=
NM_001374497.1:c.58G= NP_001361426.1:p.Gly20=
NM_001374498.1:c.58G= NP_001361427.1:p.Gly20=
NM_001374499.1:c.-476G= NP_001361428.1:n.-476G=
NM_001374500.1:c.-669G= NP_001361429.1:n.-669G=
NM_001374501.1:c.-542G= NP_001361430.1:n.-542G=
NM_001374502.1:c.-547G= NP_001361431.1:n.-547G=
NM_001374503.1:c.-612G= NP_001361432.1:n.-612G=
NR_164653.1:n.137G=
NR_164654.1:n.137G=