Canonical Allele Identifier: CA1577025613
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119479003C= , CM000667.2:g.119479003C= GRCh38
NC_000005.9:g.118814698C= , CM000667.1:g.118814698C= GRCh37
NC_000005.8:g.118842597C= NCBI36
NG_008182.1:g.31551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.604C= ENSP00000426272.2:p.Gln202=
ENST00000518349.6:c.113-17540C= ENSP00000507185.1:n.113-17540C=
ENST00000682445.1:c.*485C= ENSP00000508061.1:n.*485C=
ENST00000682531.1:n.705C=
ENST00000682626.1:c.*110C= ENSP00000507857.1:n.*110C=
ENST00000682996.1:c.604C= ENSP00000507792.1:p.Gln202=
ENST00000683265.1:n.697C=
ENST00000683371.1:c.*734C= ENSP00000508376.1:n.*734C=
ENST00000683390.1:n.2294C=
ENST00000683549.1:n.525C=
ENST00000683936.1:c.*489C= ENSP00000507721.1:n.*489C=
ENST00000683974.1:n.686C=
ENST00000683996.1:c.193C= ENSP00000507060.1:p.Gln65=
ENST00000684131.1:n.443C=
ENST00000684160.1:c.*294C= ENSP00000507821.1:n.*294C=
ENST00000684214.1:c.604C= ENSP00000508071.1:p.Gln202=
ENST00000414835.7:c.679C= ENSP00000411960.3:p.Gln227=
ENST00000510025.7:c.604C= MANE Select ENSP00000424940.3:p.Gln202=
ENST00000643250.1:c.*476C= ENSP00000494737.1:n.*476C=
ENST00000644146.1:c.*182C= ENSP00000494808.1:n.*182C=
ENST00000645099.1:c.163C= ENSP00000496091.1:p.Gln55=
ENST00000645702.1:c.193C= ENSP00000496432.1:p.Gln65=
ENST00000645832.1:c.*489C= ENSP00000494316.1:n.*489C=
ENST00000646058.1:c.604C= ENSP00000493579.1:p.Gln202=
ENST00000646355.1:c.*610C= ENSP00000493801.1:n.*610C=
ENST00000646554.1:c.*582C= ENSP00000494542.1:n.*582C=
ENST00000647335.1:c.*571C= ENSP00000495180.1:n.*571C=
ENST00000647342.1:c.*535C= ENSP00000494992.1:n.*535C=
ENST00000256216.10:c.604C= ENSP00000256216.6:p.Gln202=
ENST00000414835.6:c.184C= ENSP00000411960.2:p.Gln62=
ENST00000442060.7:c.604C= ENSP00000390208.3:p.Gln202=
ENST00000504811.5:c.679C= ENSP00000420914.1:p.Gln227=
ENST00000505181.5:n.307C=
ENST00000509514.5:c.-281C= ENSP00000426272.1:n.-281C=
ENST00000510025.5:c.532C= ENSP00000424940.1:p.Gln178=
ENST00000512644.1:n.172C=
ENST00000513628.5:c.193C= ENSP00000425993.1:p.Gln65=
ENST00000515235.6:n.664C=
ENST00000515320.5:c.550C= ENSP00000424613.1:p.Gln184=
NM_000414.3:c.604C= NP_000405.1:p.Gln202=
NM_001199291.2:c.679C= NP_001186220.1:p.Gln227=
NM_001199292.1:c.550C= NP_001186221.1:p.Gln184=
NM_001292027.1:c.532C= NP_001278956.1:p.Gln178=
NM_001292028.1:c.184C= NP_001278957.1:p.Gln62=
NM_000414.4:c.604C= MANE Select NP_000405.1:p.Gln202=
NM_001199291.3:c.679C= NP_001186220.1:p.Gln227=
NM_001199292.2:c.550C= NP_001186221.1:p.Gln184=
NM_001292027.2:c.532C= NP_001278956.1:p.Gln178=
NM_001292028.2:c.184C= NP_001278957.1:p.Gln62=
NM_001374497.1:c.595C= NP_001361426.1:p.Gln199=
NM_001374498.1:c.604C= NP_001361427.1:p.Gln202=
NM_001374499.1:c.277C= NP_001361428.1:p.Gln93=
NM_001374500.1:c.163C= NP_001361429.1:p.Gln55=
NM_001374501.1:c.193C= NP_001361430.1:p.Gln65=
NM_001374502.1:c.193C= NP_001361431.1:p.Gln65=
NM_001374503.1:c.193C= NP_001361432.1:p.Gln65=
NR_164653.1:n.683C=
NR_164654.1:n.871C=