Canonical Allele Identifier: CA446041517

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118814641A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119478946A>C , CM000667.2:g.119478946A>C	GRCh38
NC_000005.9:g.118814641A>C , CM000667.1:g.118814641A>C	GRCh37
NC_000005.8:g.118842540A>C	NCBI36
NG_008182.1:g.31494A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.547A>C	ENSP00000426272.2:p.Arg183=
ENST00000518349.6:c.113-17597A>C	ENSP00000507185.1:n.113-17597A>C
ENST00000682445.1:c.*428A>C	ENSP00000508061.1:n.*428A>C
ENST00000682531.1:n.648A>C
ENST00000682626.1:c.*53A>C	ENSP00000507857.1:n.*53A>C
ENST00000682996.1:c.547A>C	ENSP00000507792.1:p.Arg183=
ENST00000683265.1:n.640A>C
ENST00000683371.1:c.*677A>C	ENSP00000508376.1:n.*677A>C
ENST00000683390.1:n.2237A>C
ENST00000683549.1:n.468A>C
ENST00000683936.1:c.*432A>C	ENSP00000507721.1:n.*432A>C
ENST00000683974.1:n.629A>C
ENST00000683996.1:c.136A>C	ENSP00000507060.1:p.Arg46=
ENST00000684131.1:n.386A>C
ENST00000684160.1:c.*237A>C	ENSP00000507821.1:n.*237A>C
ENST00000684214.1:c.547A>C	ENSP00000508071.1:p.Arg183=
ENST00000414835.7:c.622A>C	ENSP00000411960.3:p.Arg208=
ENST00000510025.7:c.547A>C MANE Select	ENSP00000424940.3:p.Arg183=
ENST00000643250.1:c.*419A>C	ENSP00000494737.1:n.*419A>C
ENST00000644146.1:c.*125A>C	ENSP00000494808.1:n.*125A>C
ENST00000645099.1:c.106A>C	ENSP00000496091.1:p.Arg36=
ENST00000645702.1:c.136A>C	ENSP00000496432.1:p.Arg46=
ENST00000645832.1:c.*432A>C	ENSP00000494316.1:n.*432A>C
ENST00000646058.1:c.547A>C	ENSP00000493579.1:p.Arg183=
ENST00000646355.1:c.*553A>C	ENSP00000493801.1:n.*553A>C
ENST00000646554.1:c.*525A>C	ENSP00000494542.1:n.*525A>C
ENST00000647335.1:c.*514A>C	ENSP00000495180.1:n.*514A>C
ENST00000647342.1:c.*478A>C	ENSP00000494992.1:n.*478A>C
ENST00000256216.10:c.547A>C	ENSP00000256216.6:p.Arg183=
ENST00000414835.6:c.127A>C	ENSP00000411960.2:p.Arg43=
ENST00000442060.7:c.547A>C	ENSP00000390208.3:p.Arg183=
ENST00000503168.5:n.536A>C
ENST00000504811.5:c.622A>C	ENSP00000420914.1:p.Arg208=
ENST00000505181.5:n.250A>C
ENST00000509514.5:c.-338A>C	ENSP00000426272.1:n.-338A>C
ENST00000510025.5:c.475A>C	ENSP00000424940.1:p.Arg159=
ENST00000512644.1:n.115A>C
ENST00000513628.5:c.136A>C	ENSP00000425993.1:p.Arg46=
ENST00000515235.6:n.607A>C
ENST00000515320.5:c.493A>C	ENSP00000424613.1:p.Arg165=
NM_000414.3:c.547A>C	NP_000405.1:p.Arg183=
NM_001199291.2:c.622A>C	NP_001186220.1:p.Arg208=
NM_001199292.1:c.493A>C	NP_001186221.1:p.Arg165=
NM_001292027.1:c.475A>C	NP_001278956.1:p.Arg159=
NM_001292028.1:c.127A>C	NP_001278957.1:p.Arg43=
NM_000414.4:c.547A>C MANE Select	NP_000405.1:p.Arg183=
NM_001199291.3:c.622A>C	NP_001186220.1:p.Arg208=
NM_001199292.2:c.493A>C	NP_001186221.1:p.Arg165=
NM_001292027.2:c.475A>C	NP_001278956.1:p.Arg159=
NM_001292028.2:c.127A>C	NP_001278957.1:p.Arg43=
NM_001374497.1:c.538A>C	NP_001361426.1:p.Arg180=
NM_001374498.1:c.547A>C	NP_001361427.1:p.Arg183=
NM_001374499.1:c.220A>C	NP_001361428.1:p.Arg74=
NM_001374500.1:c.106A>C	NP_001361429.1:p.Arg36=
NM_001374501.1:c.136A>C	NP_001361430.1:p.Arg46=
NM_001374502.1:c.136A>C	NP_001361431.1:p.Arg46=
NM_001374503.1:c.136A>C	NP_001361432.1:p.Arg46=
NR_164653.1:n.626A>C
NR_164654.1:n.814A>C