Canonical Allele Identifier: CA360870125

Gene: HSD17B4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119529893G>A , CM000667.2:g.119529893G>A	GRCh38
NC_000005.9:g.118865588G>A , CM000667.1:g.118865588G>A	GRCh37
NC_000005.8:g.118893487G>A	NCBI36
NG_008182.1:g.82441G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.1699-1G>A	ENSP00000426272.2:n.1699-1G>A
ENST00000518349.6:c.1012-1G>A	ENSP00000507185.1:n.1012-1G>A
ENST00000520244.6:n.3506-1G>A
ENST00000682445.1:c.*1649-1G>A	ENSP00000508061.1:n.*1649-1G>A
ENST00000682531.1:n.3660-1G>A
ENST00000682626.1:c.*1274-1G>A	ENSP00000507857.1:n.*1274-1G>A
ENST00000682996.1:c.1696-1G>A	ENSP00000507792.1:n.1696-1G>A
ENST00000683265.1:n.3554-1G>A
ENST00000683335.1:n.3170-1G>A
ENST00000683371.1:c.*1898-1G>A	ENSP00000508376.1:n.*1898-1G>A
ENST00000683372.1:n.3778-1G>A
ENST00000683390.1:n.3458-1G>A
ENST00000683476.1:n.610-1G>A
ENST00000683549.1:n.3382-1G>A
ENST00000683936.1:c.*3346-1G>A	ENSP00000507721.1:n.*3346-1G>A
ENST00000683974.1:n.3497-1G>A
ENST00000683996.1:c.*978-1G>A	ENSP00000507060.1:n.*978-1G>A
ENST00000684131.1:n.3300-1G>A
ENST00000684160.1:c.*1458-1G>A	ENSP00000507821.1:n.*1458-1G>A
ENST00000684214.1:c.1768-1G>A	ENSP00000508071.1:n.1768-1G>A
ENST00000414835.7:c.1843-1G>A	ENSP00000411960.3:n.1843-1G>A
ENST00000510025.7:c.1768-1G>A MANE Select	ENSP00000424940.3:n.1768-1G>A
ENST00000643250.1:c.*1640-1G>A	ENSP00000494737.1:n.*1640-1G>A
ENST00000644146.1:c.*3039-1G>A	ENSP00000494808.1:n.*3039-1G>A
ENST00000645099.1:c.1327-1G>A	ENSP00000496091.1:n.1327-1G>A
ENST00000645702.1:c.*1171-1G>A	ENSP00000496432.1:n.*1171-1G>A
ENST00000645832.1:c.*1653-1G>A	ENSP00000494316.1:n.*1653-1G>A
ENST00000646058.1:c.1768-1G>A	ENSP00000493579.1:n.1768-1G>A
ENST00000646355.1:c.*1774-1G>A	ENSP00000493801.1:n.*1774-1G>A
ENST00000646554.1:c.*1746-1G>A	ENSP00000494542.1:n.*1746-1G>A
ENST00000647335.1:c.*1735-1G>A	ENSP00000495180.1:n.*1735-1G>A
ENST00000647342.1:c.*1699-1G>A	ENSP00000494992.1:n.*1699-1G>A
ENST00000256216.10:c.1768-1G>A	ENSP00000256216.6:n.1768-1G>A
ENST00000414835.6:c.1348-1G>A	ENSP00000411960.2:n.1348-1G>A
ENST00000442060.7:c.*330-8G>A	ENSP00000390208.3:n.*330-8G>A
ENST00000504811.5:c.1843-1G>A	ENSP00000420914.1:n.1843-1G>A
ENST00000507353.1:n.376-1G>A
ENST00000509514.5:c.982-1G>A	ENSP00000426272.1:n.982-1G>A
ENST00000509606.1:n.63-1G>A
ENST00000509951.5:n.223-1G>A
ENST00000510025.5:c.1696-1G>A	ENSP00000424940.1:n.1696-1G>A
ENST00000513628.5:c.1357-1G>A	ENSP00000425993.1:n.1357-1G>A
ENST00000515235.6:n.3521-1G>A
ENST00000515320.5:c.1714-1G>A	ENSP00000424613.1:n.1714-1G>A
ENST00000522415.5:n.435-1G>A
NM_000414.3:c.1768-1G>A	NP_000405.1:n.1768-1G>A
NM_001199291.2:c.1843-1G>A	NP_001186220.1:n.1843-1G>A
NM_001199292.1:c.1714-1G>A	NP_001186221.1:n.1714-1G>A
NM_001292027.1:c.1696-1G>A	NP_001278956.1:n.1696-1G>A
NM_001292028.1:c.1348-1G>A	NP_001278957.1:n.1348-1G>A
NM_000414.4:c.1768-1G>A MANE Select	NP_000405.1:n.1768-1G>A
NM_001199291.3:c.1843-1G>A	NP_001186220.1:n.1843-1G>A
NM_001199292.2:c.1714-1G>A	NP_001186221.1:n.1714-1G>A
NM_001292027.2:c.1696-1G>A	NP_001278956.1:n.1696-1G>A
NM_001292028.2:c.1348-1G>A	NP_001278957.1:n.1348-1G>A
NM_001374497.1:c.1759-1G>A	NP_001361426.1:n.1759-1G>A
NM_001374498.1:c.1696-1G>A	NP_001361427.1:n.1696-1G>A
NM_001374499.1:c.1441-1G>A	NP_001361428.1:n.1441-1G>A
NM_001374500.1:c.1327-1G>A	NP_001361429.1:n.1327-1G>A
NM_001374501.1:c.1357-1G>A	NP_001361430.1:n.1357-1G>A
NM_001374502.1:c.1357-1G>A	NP_001361431.1:n.1357-1G>A
NM_001374503.1:c.1357-1G>A	NP_001361432.1:n.1357-1G>A
NR_164653.1:n.1865-1G>A
NR_164654.1:n.2133-1G>A