Canonical Allele Identifier: CA2674981383

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119496466-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119496466A>G , CM000667.2:g.119496466A>G	GRCh38
NC_000005.9:g.118832161A>G , CM000667.1:g.118832161A>G	GRCh37
NC_000005.8:g.118860060A>G	NCBI36
NG_008182.1:g.49014A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000509514.6:c.869-77A>G	ENSP00000426272.2:n.869-77A>G
ENST00000518349.6:c.113-77A>G	ENSP00000507185.1:n.113-77A>G
ENST00000682445.1:c.*750-77A>G	ENSP00000508061.1:n.*750-77A>G
ENST00000682531.1:n.2761-77A>G
ENST00000682626.1:c.*375-77A>G	ENSP00000507857.1:n.*375-77A>G
ENST00000682996.1:c.869-77A>G	ENSP00000507792.1:n.869-77A>G
ENST00000683265.1:n.2655-77A>G
ENST00000683371.1:c.*999-77A>G	ENSP00000508376.1:n.*999-77A>G
ENST00000683372.1:n.2879-77A>G
ENST00000683390.1:n.2559-77A>G
ENST00000683549.1:n.2483-77A>G
ENST00000683936.1:c.*2447-77A>G	ENSP00000507721.1:n.*2447-77A>G
ENST00000683974.1:n.2644-77A>G
ENST00000683996.1:c.*79-77A>G	ENSP00000507060.1:n.*79-77A>G
ENST00000684131.1:n.2401-77A>G
ENST00000684160.1:c.*559-77A>G	ENSP00000507821.1:n.*559-77A>G
ENST00000684214.1:c.869-77A>G	ENSP00000508071.1:n.869-77A>G
ENST00000414835.7:c.944-77A>G	ENSP00000411960.3:n.944-77A>G
ENST00000510025.7:c.869-77A>G MANE Select	ENSP00000424940.3:n.869-77A>G
ENST00000643250.1:c.*741-77A>G	ENSP00000494737.1:n.*741-77A>G
ENST00000644146.1:c.*2140-77A>G	ENSP00000494808.1:n.*2140-77A>G
ENST00000645099.1:c.428-77A>G	ENSP00000496091.1:n.428-77A>G
ENST00000645702.1:c.*272-77A>G	ENSP00000496432.1:n.*272-77A>G
ENST00000645832.1:c.*754-77A>G	ENSP00000494316.1:n.*754-77A>G
ENST00000646058.1:c.869-77A>G	ENSP00000493579.1:n.869-77A>G
ENST00000646355.1:c.*875-77A>G	ENSP00000493801.1:n.*875-77A>G
ENST00000646554.1:c.*847-77A>G	ENSP00000494542.1:n.*847-77A>G
ENST00000647335.1:c.*836-77A>G	ENSP00000495180.1:n.*836-77A>G
ENST00000647342.1:c.*800-77A>G	ENSP00000494992.1:n.*800-77A>G
ENST00000256216.10:c.869-77A>G	ENSP00000256216.6:n.869-77A>G
ENST00000414835.6:c.449-77A>G	ENSP00000411960.2:n.449-77A>G
ENST00000442060.7:c.869-77A>G	ENSP00000390208.3:n.869-77A>G
ENST00000504811.5:c.944-77A>G	ENSP00000420914.1:n.944-77A>G
ENST00000509514.5:c.83-77A>G	ENSP00000426272.1:n.83-77A>G
ENST00000510025.5:c.797-77A>G	ENSP00000424940.1:n.797-77A>G
ENST00000513628.5:c.458-77A>G	ENSP00000425993.1:n.458-77A>G
ENST00000515235.6:n.2622-77A>G
ENST00000515320.5:c.815-77A>G	ENSP00000424613.1:n.815-77A>G
ENST00000520216.5:n.130-77A>G
NM_000414.3:c.869-77A>G	NP_000405.1:n.869-77A>G
NM_001199291.2:c.944-77A>G	NP_001186220.1:n.944-77A>G
NM_001199292.1:c.815-77A>G	NP_001186221.1:n.815-77A>G
NM_001292027.1:c.797-77A>G	NP_001278956.1:n.797-77A>G
NM_001292028.1:c.449-77A>G	NP_001278957.1:n.449-77A>G
NM_000414.4:c.869-77A>G MANE Select	NP_000405.1:n.869-77A>G
NM_001199291.3:c.944-77A>G	NP_001186220.1:n.944-77A>G
NM_001199292.2:c.815-77A>G	NP_001186221.1:n.815-77A>G
NM_001292027.2:c.797-77A>G	NP_001278956.1:n.797-77A>G
NM_001292028.2:c.449-77A>G	NP_001278957.1:n.449-77A>G
NM_001374497.1:c.860-77A>G	NP_001361426.1:n.860-77A>G
NM_001374498.1:c.869-77A>G	NP_001361427.1:n.869-77A>G
NM_001374499.1:c.542-77A>G	NP_001361428.1:n.542-77A>G
NM_001374500.1:c.428-77A>G	NP_001361429.1:n.428-77A>G
NM_001374501.1:c.458-77A>G	NP_001361430.1:n.458-77A>G
NM_001374502.1:c.458-77A>G	NP_001361431.1:n.458-77A>G
NM_001374503.1:c.458-77A>G	NP_001361432.1:n.458-77A>G
NR_164653.1:n.966-77A>G
NR_164654.1:n.1234-77A>G