Canonical Allele Identifier: CA446041418
Gene: HSD17B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.118814565C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478870C>A , CM000667.2:g.119478870C>A GRCh38
NC_000005.9:g.118814565C>A , CM000667.1:g.118814565C>A GRCh37
NC_000005.8:g.118842464C>A NCBI36
NG_008182.1:g.31418C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.471C>A ENSP00000426272.2:p.Gly157=
ENST00000518349.6:c.113-17673C>A ENSP00000507185.1:n.113-17673C>A
ENST00000682445.1:c.*352C>A ENSP00000508061.1:n.*352C>A
ENST00000682531.1:n.572C>A
ENST00000682626.1:c.499C>A ENSP00000507857.1:p.Gln167Lys
ENST00000682996.1:c.471C>A ENSP00000507792.1:p.Gly157=
ENST00000683265.1:n.564C>A
ENST00000683371.1:c.*601C>A ENSP00000508376.1:n.*601C>A
ENST00000683390.1:n.2161C>A
ENST00000683549.1:n.392C>A
ENST00000683936.1:c.*356C>A ENSP00000507721.1:n.*356C>A
ENST00000683974.1:n.553C>A
ENST00000683996.1:c.60C>A ENSP00000507060.1:p.Gly20=
ENST00000684131.1:n.310C>A
ENST00000684160.1:c.*161C>A ENSP00000507821.1:n.*161C>A
ENST00000684214.1:c.471C>A ENSP00000508071.1:p.Gly157=
ENST00000414835.7:c.546C>A ENSP00000411960.3:p.Gly182=
ENST00000510025.7:c.471C>A MANE Select ENSP00000424940.3:p.Gly157=
ENST00000643250.1:c.*343C>A ENSP00000494737.1:n.*343C>A
ENST00000644146.1:c.*49C>A ENSP00000494808.1:n.*49C>A
ENST00000645099.1:c.30C>A ENSP00000496091.1:p.Gly10=
ENST00000645702.1:c.60C>A ENSP00000496432.1:p.Gly20=
ENST00000645832.1:c.*356C>A ENSP00000494316.1:n.*356C>A
ENST00000646058.1:c.471C>A ENSP00000493579.1:p.Gly157=
ENST00000646355.1:c.*477C>A ENSP00000493801.1:n.*477C>A
ENST00000646554.1:c.*449C>A ENSP00000494542.1:n.*449C>A
ENST00000646590.1:c.462C>A ENSP00000494892.1:p.Gly154=
ENST00000647335.1:c.*438C>A ENSP00000495180.1:n.*438C>A
ENST00000647342.1:c.*402C>A ENSP00000494992.1:n.*402C>A
ENST00000256216.10:c.471C>A ENSP00000256216.6:p.Gly157=
ENST00000414835.6:c.51C>A ENSP00000411960.2:p.Gly17=
ENST00000442060.7:c.471C>A ENSP00000390208.3:p.Gly157=
ENST00000503168.5:n.460C>A
ENST00000504811.5:c.546C>A ENSP00000420914.1:p.Gly182=
ENST00000505181.5:n.174C>A
ENST00000508788.5:n.373C>A
ENST00000509514.5:c.-414C>A ENSP00000426272.1:n.-414C>A
ENST00000510025.5:c.399C>A ENSP00000424940.1:p.Gly133=
ENST00000512644.1:n.39C>A
ENST00000512841.5:n.519C>A
ENST00000513628.5:c.60C>A ENSP00000425993.1:p.Gly20=
ENST00000515235.6:n.531C>A
ENST00000515320.5:c.417C>A ENSP00000424613.1:p.Gly139=
NM_000414.3:c.471C>A NP_000405.1:p.Gly157=
NM_001199291.2:c.546C>A NP_001186220.1:p.Gly182=
NM_001199292.1:c.417C>A NP_001186221.1:p.Gly139=
NM_001292027.1:c.399C>A NP_001278956.1:p.Gly133=
NM_001292028.1:c.51C>A NP_001278957.1:p.Gly17=
NM_000414.4:c.471C>A MANE Select NP_000405.1:p.Gly157=
NM_001199291.3:c.546C>A NP_001186220.1:p.Gly182=
NM_001199292.2:c.417C>A NP_001186221.1:p.Gly139=
NM_001292027.2:c.399C>A NP_001278956.1:p.Gly133=
NM_001292028.2:c.51C>A NP_001278957.1:p.Gly17=
NM_001374497.1:c.462C>A NP_001361426.1:p.Gly154=
NM_001374498.1:c.471C>A NP_001361427.1:p.Gly157=
NM_001374499.1:c.144C>A NP_001361428.1:p.Gly48=
NM_001374500.1:c.30C>A NP_001361429.1:p.Gly10=
NM_001374501.1:c.60C>A NP_001361430.1:p.Gly20=
NM_001374502.1:c.60C>A NP_001361431.1:p.Gly20=
NM_001374503.1:c.60C>A NP_001361432.1:p.Gly20=
NR_164653.1:n.550C>A
NR_164654.1:n.738C>A