Canonical Allele Identifier: CA360866209
Gene: HSD17B4 HGNC NCBI

Linked Data

dbSNP Id: rs1202368985

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478902A>G , CM000667.2:g.119478902A>G GRCh38
NC_000005.9:g.118814597A>G , CM000667.1:g.118814597A>G GRCh37
NC_000005.8:g.118842496A>G NCBI36
NG_008182.1:g.31450A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.503A>G ENSP00000426272.2:p.Lys168Arg
ENST00000518349.6:c.113-17641A>G ENSP00000507185.1:n.113-17641A>G
ENST00000682445.1:c.*384A>G ENSP00000508061.1:n.*384A>G
ENST00000682531.1:n.604A>G
ENST00000682626.1:c.*9A>G ENSP00000507857.1:n.*9A>G
ENST00000682996.1:c.503A>G ENSP00000507792.1:p.Lys168Arg
ENST00000683265.1:n.596A>G
ENST00000683371.1:c.*633A>G ENSP00000508376.1:n.*633A>G
ENST00000683390.1:n.2193A>G
ENST00000683549.1:n.424A>G
ENST00000683936.1:c.*388A>G ENSP00000507721.1:n.*388A>G
ENST00000683974.1:n.585A>G
ENST00000683996.1:c.92A>G ENSP00000507060.1:p.Lys31Arg
ENST00000684131.1:n.342A>G
ENST00000684160.1:c.*193A>G ENSP00000507821.1:n.*193A>G
ENST00000684214.1:c.503A>G ENSP00000508071.1:p.Lys168Arg
ENST00000414835.7:c.578A>G ENSP00000411960.3:p.Lys193Arg
ENST00000510025.7:c.503A>G MANE Select ENSP00000424940.3:p.Lys168Arg
ENST00000643250.1:c.*375A>G ENSP00000494737.1:n.*375A>G
ENST00000644146.1:c.*81A>G ENSP00000494808.1:n.*81A>G
ENST00000645099.1:c.62A>G ENSP00000496091.1:p.Lys21Arg
ENST00000645702.1:c.92A>G ENSP00000496432.1:p.Lys31Arg
ENST00000645832.1:c.*388A>G ENSP00000494316.1:n.*388A>G
ENST00000646058.1:c.503A>G ENSP00000493579.1:p.Lys168Arg
ENST00000646355.1:c.*509A>G ENSP00000493801.1:n.*509A>G
ENST00000646554.1:c.*481A>G ENSP00000494542.1:n.*481A>G
ENST00000646590.1:c.494A>G ENSP00000494892.1:p.Lys165Arg
ENST00000647335.1:c.*470A>G ENSP00000495180.1:n.*470A>G
ENST00000647342.1:c.*434A>G ENSP00000494992.1:n.*434A>G
ENST00000256216.10:c.503A>G ENSP00000256216.6:p.Lys168Arg
ENST00000414835.6:c.83A>G ENSP00000411960.2:p.Lys28Arg
ENST00000442060.7:c.503A>G ENSP00000390208.3:p.Lys168Arg
ENST00000503168.5:n.492A>G
ENST00000504811.5:c.578A>G ENSP00000420914.1:p.Lys193Arg
ENST00000505181.5:n.206A>G
ENST00000508788.5:n.405A>G
ENST00000509514.5:c.-382A>G ENSP00000426272.1:n.-382A>G
ENST00000510025.5:c.431A>G ENSP00000424940.1:p.Lys144Arg
ENST00000512644.1:n.71A>G
ENST00000512841.5:n.551A>G
ENST00000513628.5:c.92A>G ENSP00000425993.1:p.Lys31Arg
ENST00000515235.6:n.563A>G
ENST00000515320.5:c.449A>G ENSP00000424613.1:p.Lys150Arg
NM_000414.3:c.503A>G NP_000405.1:p.Lys168Arg
NM_001199291.2:c.578A>G NP_001186220.1:p.Lys193Arg
NM_001199292.1:c.449A>G NP_001186221.1:p.Lys150Arg
NM_001292027.1:c.431A>G NP_001278956.1:p.Lys144Arg
NM_001292028.1:c.83A>G NP_001278957.1:p.Lys28Arg
NM_000414.4:c.503A>G MANE Select NP_000405.1:p.Lys168Arg
NM_001199291.3:c.578A>G NP_001186220.1:p.Lys193Arg
NM_001199292.2:c.449A>G NP_001186221.1:p.Lys150Arg
NM_001292027.2:c.431A>G NP_001278956.1:p.Lys144Arg
NM_001292028.2:c.83A>G NP_001278957.1:p.Lys28Arg
NM_001374497.1:c.494A>G NP_001361426.1:p.Lys165Arg
NM_001374498.1:c.503A>G NP_001361427.1:p.Lys168Arg
NM_001374499.1:c.176A>G NP_001361428.1:p.Lys59Arg
NM_001374500.1:c.62A>G NP_001361429.1:p.Lys21Arg
NM_001374501.1:c.92A>G NP_001361430.1:p.Lys31Arg
NM_001374502.1:c.92A>G NP_001361431.1:p.Lys31Arg
NM_001374503.1:c.92A>G NP_001361432.1:p.Lys31Arg
NR_164653.1:n.582A>G
NR_164654.1:n.770A>G