Canonical Allele Identifier: CA360866354

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118814665A>T (hg19) ; chr5:g.119478970A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119478970A>T , CM000667.2:g.119478970A>T	GRCh38
NC_000005.9:g.118814665A>T , CM000667.1:g.118814665A>T	GRCh37
NC_000005.8:g.118842564A>T	NCBI36
NG_008182.1:g.31518A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.571A>T	ENSP00000426272.2:p.Thr191Ser
ENST00000518349.6:c.113-17573A>T	ENSP00000507185.1:n.113-17573A>T
ENST00000682445.1:c.*452A>T	ENSP00000508061.1:n.*452A>T
ENST00000682531.1:n.672A>T
ENST00000682626.1:c.*77A>T	ENSP00000507857.1:n.*77A>T
ENST00000682996.1:c.571A>T	ENSP00000507792.1:p.Thr191Ser
ENST00000683265.1:n.664A>T
ENST00000683371.1:c.*701A>T	ENSP00000508376.1:n.*701A>T
ENST00000683390.1:n.2261A>T
ENST00000683549.1:n.492A>T
ENST00000683936.1:c.*456A>T	ENSP00000507721.1:n.*456A>T
ENST00000683974.1:n.653A>T
ENST00000683996.1:c.160A>T	ENSP00000507060.1:p.Thr54Ser
ENST00000684131.1:n.410A>T
ENST00000684160.1:c.*261A>T	ENSP00000507821.1:n.*261A>T
ENST00000684214.1:c.571A>T	ENSP00000508071.1:p.Thr191Ser
ENST00000414835.7:c.646A>T	ENSP00000411960.3:p.Thr216Ser
ENST00000510025.7:c.571A>T MANE Select	ENSP00000424940.3:p.Thr191Ser
ENST00000643250.1:c.*443A>T	ENSP00000494737.1:n.*443A>T
ENST00000644146.1:c.*149A>T	ENSP00000494808.1:n.*149A>T
ENST00000645099.1:c.130A>T	ENSP00000496091.1:p.Thr44Ser
ENST00000645702.1:c.160A>T	ENSP00000496432.1:p.Thr54Ser
ENST00000645832.1:c.*456A>T	ENSP00000494316.1:n.*456A>T
ENST00000646058.1:c.571A>T	ENSP00000493579.1:p.Thr191Ser
ENST00000646355.1:c.*577A>T	ENSP00000493801.1:n.*577A>T
ENST00000646554.1:c.*549A>T	ENSP00000494542.1:n.*549A>T
ENST00000647335.1:c.*538A>T	ENSP00000495180.1:n.*538A>T
ENST00000647342.1:c.*502A>T	ENSP00000494992.1:n.*502A>T
ENST00000256216.10:c.571A>T	ENSP00000256216.6:p.Thr191Ser
ENST00000414835.6:c.151A>T	ENSP00000411960.2:p.Thr51Ser
ENST00000442060.7:c.571A>T	ENSP00000390208.3:p.Thr191Ser
ENST00000503168.5:n.560A>T
ENST00000504811.5:c.646A>T	ENSP00000420914.1:p.Thr216Ser
ENST00000505181.5:n.274A>T
ENST00000509514.5:c.-314A>T	ENSP00000426272.1:n.-314A>T
ENST00000510025.5:c.499A>T	ENSP00000424940.1:p.Thr167Ser
ENST00000512644.1:n.139A>T
ENST00000513628.5:c.160A>T	ENSP00000425993.1:p.Thr54Ser
ENST00000515235.6:n.631A>T
ENST00000515320.5:c.517A>T	ENSP00000424613.1:p.Thr173Ser
NM_000414.3:c.571A>T	NP_000405.1:p.Thr191Ser
NM_001199291.2:c.646A>T	NP_001186220.1:p.Thr216Ser
NM_001199292.1:c.517A>T	NP_001186221.1:p.Thr173Ser
NM_001292027.1:c.499A>T	NP_001278956.1:p.Thr167Ser
NM_001292028.1:c.151A>T	NP_001278957.1:p.Thr51Ser
NM_000414.4:c.571A>T MANE Select	NP_000405.1:p.Thr191Ser
NM_001199291.3:c.646A>T	NP_001186220.1:p.Thr216Ser
NM_001199292.2:c.517A>T	NP_001186221.1:p.Thr173Ser
NM_001292027.2:c.499A>T	NP_001278956.1:p.Thr167Ser
NM_001292028.2:c.151A>T	NP_001278957.1:p.Thr51Ser
NM_001374497.1:c.562A>T	NP_001361426.1:p.Thr188Ser
NM_001374498.1:c.571A>T	NP_001361427.1:p.Thr191Ser
NM_001374499.1:c.244A>T	NP_001361428.1:p.Thr82Ser
NM_001374500.1:c.130A>T	NP_001361429.1:p.Thr44Ser
NM_001374501.1:c.160A>T	NP_001361430.1:p.Thr54Ser
NM_001374502.1:c.160A>T	NP_001361431.1:p.Thr54Ser
NM_001374503.1:c.160A>T	NP_001361432.1:p.Thr54Ser
NR_164653.1:n.650A>T
NR_164654.1:n.838A>T