Canonical Allele Identifier: CA3382331
Gene: HSD17B4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119525916G>A , CM000667.2:g.119525916G>A GRCh38
NC_000005.9:g.118861611G>A , CM000667.1:g.118861611G>A GRCh37
NC_000005.8:g.118889510G>A NCBI36
NG_008182.1:g.78464G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.1505-1G>A ENSP00000426272.2:n.1505-1G>A
ENST00000518349.6:c.818-1G>A ENSP00000507185.1:n.818-1G>A
ENST00000520244.6:n.3312-1G>A
ENST00000682445.1:c.*1455-1G>A ENSP00000508061.1:n.*1455-1G>A
ENST00000682531.1:n.3466-1G>A
ENST00000682626.1:c.*1080-1G>A ENSP00000507857.1:n.*1080-1G>A
ENST00000682996.1:c.1502-1G>A ENSP00000507792.1:n.1502-1G>A
ENST00000683265.1:n.3360-1G>A
ENST00000683335.1:n.2976-1G>A
ENST00000683371.1:c.*1704-1G>A ENSP00000508376.1:n.*1704-1G>A
ENST00000683372.1:n.3584-1G>A
ENST00000683390.1:n.3264-1G>A
ENST00000683476.1:n.416-1G>A
ENST00000683549.1:n.3188-1G>A
ENST00000683936.1:c.*3152-1G>A ENSP00000507721.1:n.*3152-1G>A
ENST00000683974.1:n.3303-1G>A
ENST00000683996.1:c.*784-1G>A ENSP00000507060.1:n.*784-1G>A
ENST00000684131.1:n.3106-1G>A
ENST00000684160.1:c.*1264-1G>A ENSP00000507821.1:n.*1264-1G>A
ENST00000684214.1:c.1574-1G>A ENSP00000508071.1:n.1574-1G>A
ENST00000414835.7:c.1649-1G>A ENSP00000411960.3:n.1649-1G>A
ENST00000510025.7:c.1574-1G>A MANE Select ENSP00000424940.3:n.1574-1G>A
ENST00000643250.1:c.*1446-1G>A ENSP00000494737.1:n.*1446-1G>A
ENST00000644146.1:c.*2845-1G>A ENSP00000494808.1:n.*2845-1G>A
ENST00000645099.1:c.1133-1G>A ENSP00000496091.1:n.1133-1G>A
ENST00000645702.1:c.*977-1G>A ENSP00000496432.1:n.*977-1G>A
ENST00000645832.1:c.*1459-1G>A ENSP00000494316.1:n.*1459-1G>A
ENST00000646058.1:c.1574-1G>A ENSP00000493579.1:n.1574-1G>A
ENST00000646355.1:c.*1580-1G>A ENSP00000493801.1:n.*1580-1G>A
ENST00000646554.1:c.*1552-1G>A ENSP00000494542.1:n.*1552-1G>A
ENST00000647335.1:c.*1541-1G>A ENSP00000495180.1:n.*1541-1G>A
ENST00000647342.1:c.*1505-1G>A ENSP00000494992.1:n.*1505-1G>A
ENST00000256216.10:c.1574-1G>A ENSP00000256216.6:n.1574-1G>A
ENST00000414835.6:c.1154-1G>A ENSP00000411960.2:n.1154-1G>A
ENST00000442060.7:c.*136-1G>A ENSP00000390208.3:n.*136-1G>A
ENST00000504811.5:c.1649-1G>A ENSP00000420914.1:n.1649-1G>A
ENST00000507353.1:n.181G>A
ENST00000509514.5:c.788-1G>A ENSP00000426272.1:n.788-1G>A
ENST00000509951.5:n.29-1G>A
ENST00000510025.5:c.1502-1G>A ENSP00000424940.1:n.1502-1G>A
ENST00000513628.5:c.1163-1G>A ENSP00000425993.1:n.1163-1G>A
ENST00000515235.6:n.3327-1G>A
ENST00000515320.5:c.1520-1G>A ENSP00000424613.1:n.1520-1G>A
ENST00000518349.5:n.708-1G>A
ENST00000520244.5:n.357-1G>A
ENST00000522415.5:n.241-1G>A
NM_000414.3:c.1574-1G>A NP_000405.1:n.1574-1G>A
NM_001199291.2:c.1649-1G>A NP_001186220.1:n.1649-1G>A
NM_001199292.1:c.1520-1G>A NP_001186221.1:n.1520-1G>A
NM_001292027.1:c.1502-1G>A NP_001278956.1:n.1502-1G>A
NM_001292028.1:c.1154-1G>A NP_001278957.1:n.1154-1G>A
NM_000414.4:c.1574-1G>A MANE Select NP_000405.1:n.1574-1G>A
NM_001199291.3:c.1649-1G>A NP_001186220.1:n.1649-1G>A
NM_001199292.2:c.1520-1G>A NP_001186221.1:n.1520-1G>A
NM_001292027.2:c.1502-1G>A NP_001278956.1:n.1502-1G>A
NM_001292028.2:c.1154-1G>A NP_001278957.1:n.1154-1G>A
NM_001374497.1:c.1565-1G>A NP_001361426.1:n.1565-1G>A
NM_001374498.1:c.1502-1G>A NP_001361427.1:n.1502-1G>A
NM_001374499.1:c.1247-1G>A NP_001361428.1:n.1247-1G>A
NM_001374500.1:c.1133-1G>A NP_001361429.1:n.1133-1G>A
NM_001374501.1:c.1163-1G>A NP_001361430.1:n.1163-1G>A
NM_001374502.1:c.1163-1G>A NP_001361431.1:n.1163-1G>A
NM_001374503.1:c.1163-1G>A NP_001361432.1:n.1163-1G>A
NR_164653.1:n.1671-1G>A
NR_164654.1:n.1939-1G>A
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