Canonical Allele Identifier: CA360866324
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478957C>A , CM000667.2:g.119478957C>A GRCh38
NC_000005.9:g.118814652C>A , CM000667.1:g.118814652C>A GRCh37
NC_000005.8:g.118842551C>A NCBI36
NG_008182.1:g.31505C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.558C>A ENSP00000426272.2:p.Asn186Lys
ENST00000518349.6:c.113-17586C>A ENSP00000507185.1:n.113-17586C>A
ENST00000682445.1:c.*439C>A ENSP00000508061.1:n.*439C>A
ENST00000682531.1:n.659C>A
ENST00000682626.1:c.*64C>A ENSP00000507857.1:n.*64C>A
ENST00000682996.1:c.558C>A ENSP00000507792.1:p.Asn186Lys
ENST00000683265.1:n.651C>A
ENST00000683371.1:c.*688C>A ENSP00000508376.1:n.*688C>A
ENST00000683390.1:n.2248C>A
ENST00000683549.1:n.479C>A
ENST00000683936.1:c.*443C>A ENSP00000507721.1:n.*443C>A
ENST00000683974.1:n.640C>A
ENST00000683996.1:c.147C>A ENSP00000507060.1:p.Asn49Lys
ENST00000684131.1:n.397C>A
ENST00000684160.1:c.*248C>A ENSP00000507821.1:n.*248C>A
ENST00000684214.1:c.558C>A ENSP00000508071.1:p.Asn186Lys
ENST00000414835.7:c.633C>A ENSP00000411960.3:p.Asn211Lys
ENST00000510025.7:c.558C>A MANE Select ENSP00000424940.3:p.Asn186Lys
ENST00000643250.1:c.*430C>A ENSP00000494737.1:n.*430C>A
ENST00000644146.1:c.*136C>A ENSP00000494808.1:n.*136C>A
ENST00000645099.1:c.117C>A ENSP00000496091.1:p.Asn39Lys
ENST00000645702.1:c.147C>A ENSP00000496432.1:p.Asn49Lys
ENST00000645832.1:c.*443C>A ENSP00000494316.1:n.*443C>A
ENST00000646058.1:c.558C>A ENSP00000493579.1:p.Asn186Lys
ENST00000646355.1:c.*564C>A ENSP00000493801.1:n.*564C>A
ENST00000646554.1:c.*536C>A ENSP00000494542.1:n.*536C>A
ENST00000647335.1:c.*525C>A ENSP00000495180.1:n.*525C>A
ENST00000647342.1:c.*489C>A ENSP00000494992.1:n.*489C>A
ENST00000256216.10:c.558C>A ENSP00000256216.6:p.Asn186Lys
ENST00000414835.6:c.138C>A ENSP00000411960.2:p.Asn46Lys
ENST00000442060.7:c.558C>A ENSP00000390208.3:p.Asn186Lys
ENST00000503168.5:n.547C>A
ENST00000504811.5:c.633C>A ENSP00000420914.1:p.Asn211Lys
ENST00000505181.5:n.261C>A
ENST00000509514.5:c.-327C>A ENSP00000426272.1:n.-327C>A
ENST00000510025.5:c.486C>A ENSP00000424940.1:p.Asn162Lys
ENST00000512644.1:n.126C>A
ENST00000513628.5:c.147C>A ENSP00000425993.1:p.Asn49Lys
ENST00000515235.6:n.618C>A
ENST00000515320.5:c.504C>A ENSP00000424613.1:p.Asn168Lys
NM_000414.3:c.558C>A NP_000405.1:p.Asn186Lys
NM_001199291.2:c.633C>A NP_001186220.1:p.Asn211Lys
NM_001199292.1:c.504C>A NP_001186221.1:p.Asn168Lys
NM_001292027.1:c.486C>A NP_001278956.1:p.Asn162Lys
NM_001292028.1:c.138C>A NP_001278957.1:p.Asn46Lys
NM_000414.4:c.558C>A MANE Select NP_000405.1:p.Asn186Lys
NM_001199291.3:c.633C>A NP_001186220.1:p.Asn211Lys
NM_001199292.2:c.504C>A NP_001186221.1:p.Asn168Lys
NM_001292027.2:c.486C>A NP_001278956.1:p.Asn162Lys
NM_001292028.2:c.138C>A NP_001278957.1:p.Asn46Lys
NM_001374497.1:c.549C>A NP_001361426.1:p.Asn183Lys
NM_001374498.1:c.558C>A NP_001361427.1:p.Asn186Lys
NM_001374499.1:c.231C>A NP_001361428.1:p.Asn77Lys
NM_001374500.1:c.117C>A NP_001361429.1:p.Asn39Lys
NM_001374501.1:c.147C>A NP_001361430.1:p.Asn49Lys
NM_001374502.1:c.147C>A NP_001361431.1:p.Asn49Lys
NM_001374503.1:c.147C>A NP_001361432.1:p.Asn49Lys
NR_164653.1:n.637C>A
NR_164654.1:n.825C>A