Canonical Allele Identifier: CA360866075
Gene: HSD17B4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119478843G>C , CM000667.2:g.119478843G>C GRCh38
NC_000005.9:g.118814538G>C , CM000667.1:g.118814538G>C GRCh37
NC_000005.8:g.118842437G>C NCBI36
NG_008182.1:g.31391G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000509514.6:c.444G>C ENSP00000426272.2:p.Met148Ile
ENST00000518349.6:c.113-17700G>C ENSP00000507185.1:n.113-17700G>C
ENST00000682445.1:c.*325G>C ENSP00000508061.1:n.*325G>C
ENST00000682531.1:n.545G>C
ENST00000682626.1:c.472G>C ENSP00000507857.1:p.Asp158His
ENST00000682996.1:c.444G>C ENSP00000507792.1:p.Met148Ile
ENST00000683265.1:n.537G>C
ENST00000683371.1:c.*574G>C ENSP00000508376.1:n.*574G>C
ENST00000683390.1:n.2134G>C
ENST00000683549.1:n.365G>C
ENST00000683936.1:c.*329G>C ENSP00000507721.1:n.*329G>C
ENST00000683974.1:n.526G>C
ENST00000683996.1:c.33G>C ENSP00000507060.1:p.Met11Ile
ENST00000684131.1:n.283G>C
ENST00000684160.1:c.*134G>C ENSP00000507821.1:n.*134G>C
ENST00000684214.1:c.444G>C ENSP00000508071.1:p.Met148Ile
ENST00000414835.7:c.519G>C ENSP00000411960.3:p.Met173Ile
ENST00000510025.7:c.444G>C MANE Select ENSP00000424940.3:p.Met148Ile
ENST00000643250.1:c.*316G>C ENSP00000494737.1:n.*316G>C
ENST00000644146.1:c.*22G>C ENSP00000494808.1:n.*22G>C
ENST00000645099.1:c.3G>C ENSP00000496091.1:p.Met1Ile
ENST00000645702.1:c.33G>C ENSP00000496432.1:p.Met11Ile
ENST00000645832.1:c.*329G>C ENSP00000494316.1:n.*329G>C
ENST00000646058.1:c.444G>C ENSP00000493579.1:p.Met148Ile
ENST00000646355.1:c.*450G>C ENSP00000493801.1:n.*450G>C
ENST00000646554.1:c.*422G>C ENSP00000494542.1:n.*422G>C
ENST00000646590.1:c.435G>C ENSP00000494892.1:p.Met145Ile
ENST00000647335.1:c.*411G>C ENSP00000495180.1:n.*411G>C
ENST00000647342.1:c.*375G>C ENSP00000494992.1:n.*375G>C
ENST00000256216.10:c.444G>C ENSP00000256216.6:p.Met148Ile
ENST00000414835.6:c.24G>C ENSP00000411960.2:p.Met8Ile
ENST00000442060.7:c.444G>C ENSP00000390208.3:p.Met148Ile
ENST00000503168.5:n.433G>C
ENST00000504811.5:c.519G>C ENSP00000420914.1:p.Met173Ile
ENST00000505181.5:n.147G>C
ENST00000508788.5:n.346G>C
ENST00000509514.5:c.-441G>C ENSP00000426272.1:n.-441G>C
ENST00000510025.5:c.372G>C ENSP00000424940.1:p.Met124Ile
ENST00000512644.1:n.12G>C
ENST00000512841.5:n.492G>C
ENST00000513628.5:c.33G>C ENSP00000425993.1:p.Met11Ile
ENST00000515235.6:n.504G>C
ENST00000515320.5:c.390G>C ENSP00000424613.1:p.Met130Ile
NM_000414.3:c.444G>C NP_000405.1:p.Met148Ile
NM_001199291.2:c.519G>C NP_001186220.1:p.Met173Ile
NM_001199292.1:c.390G>C NP_001186221.1:p.Met130Ile
NM_001292027.1:c.372G>C NP_001278956.1:p.Met124Ile
NM_001292028.1:c.24G>C NP_001278957.1:p.Met8Ile
NM_000414.4:c.444G>C MANE Select NP_000405.1:p.Met148Ile
NM_001199291.3:c.519G>C NP_001186220.1:p.Met173Ile
NM_001199292.2:c.390G>C NP_001186221.1:p.Met130Ile
NM_001292027.2:c.372G>C NP_001278956.1:p.Met124Ile
NM_001292028.2:c.24G>C NP_001278957.1:p.Met8Ile
NM_001374497.1:c.435G>C NP_001361426.1:p.Met145Ile
NM_001374498.1:c.444G>C NP_001361427.1:p.Met148Ile
NM_001374499.1:c.117G>C NP_001361428.1:p.Met39Ile
NM_001374500.1:c.3G>C NP_001361429.1:p.Met1Ile
NM_001374501.1:c.33G>C NP_001361430.1:p.Met11Ile
NM_001374502.1:c.33G>C NP_001361431.1:p.Met11Ile
NM_001374503.1:c.33G>C NP_001361432.1:p.Met11Ile
NR_164653.1:n.523G>C
NR_164654.1:n.711G>C