Canonical Allele Identifier: CA446041519

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118814646A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119478951A>G , CM000667.2:g.119478951A>G	GRCh38
NC_000005.9:g.118814646A>G , CM000667.1:g.118814646A>G	GRCh37
NC_000005.8:g.118842545A>G	NCBI36
NG_008182.1:g.31499A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.552A>G	ENSP00000426272.2:p.Lys184=
ENST00000518349.6:c.113-17592A>G	ENSP00000507185.1:n.113-17592A>G
ENST00000682445.1:c.*433A>G	ENSP00000508061.1:n.*433A>G
ENST00000682531.1:n.653A>G
ENST00000682626.1:c.*58A>G	ENSP00000507857.1:n.*58A>G
ENST00000682996.1:c.552A>G	ENSP00000507792.1:p.Lys184=
ENST00000683265.1:n.645A>G
ENST00000683371.1:c.*682A>G	ENSP00000508376.1:n.*682A>G
ENST00000683390.1:n.2242A>G
ENST00000683549.1:n.473A>G
ENST00000683936.1:c.*437A>G	ENSP00000507721.1:n.*437A>G
ENST00000683974.1:n.634A>G
ENST00000683996.1:c.141A>G	ENSP00000507060.1:p.Lys47=
ENST00000684131.1:n.391A>G
ENST00000684160.1:c.*242A>G	ENSP00000507821.1:n.*242A>G
ENST00000684214.1:c.552A>G	ENSP00000508071.1:p.Lys184=
ENST00000414835.7:c.627A>G	ENSP00000411960.3:p.Lys209=
ENST00000510025.7:c.552A>G MANE Select	ENSP00000424940.3:p.Lys184=
ENST00000643250.1:c.*424A>G	ENSP00000494737.1:n.*424A>G
ENST00000644146.1:c.*130A>G	ENSP00000494808.1:n.*130A>G
ENST00000645099.1:c.111A>G	ENSP00000496091.1:p.Lys37=
ENST00000645702.1:c.141A>G	ENSP00000496432.1:p.Lys47=
ENST00000645832.1:c.*437A>G	ENSP00000494316.1:n.*437A>G
ENST00000646058.1:c.552A>G	ENSP00000493579.1:p.Lys184=
ENST00000646355.1:c.*558A>G	ENSP00000493801.1:n.*558A>G
ENST00000646554.1:c.*530A>G	ENSP00000494542.1:n.*530A>G
ENST00000647335.1:c.*519A>G	ENSP00000495180.1:n.*519A>G
ENST00000647342.1:c.*483A>G	ENSP00000494992.1:n.*483A>G
ENST00000256216.10:c.552A>G	ENSP00000256216.6:p.Lys184=
ENST00000414835.6:c.132A>G	ENSP00000411960.2:p.Lys44=
ENST00000442060.7:c.552A>G	ENSP00000390208.3:p.Lys184=
ENST00000503168.5:n.541A>G
ENST00000504811.5:c.627A>G	ENSP00000420914.1:p.Lys209=
ENST00000505181.5:n.255A>G
ENST00000509514.5:c.-333A>G	ENSP00000426272.1:n.-333A>G
ENST00000510025.5:c.480A>G	ENSP00000424940.1:p.Lys160=
ENST00000512644.1:n.120A>G
ENST00000513628.5:c.141A>G	ENSP00000425993.1:p.Lys47=
ENST00000515235.6:n.612A>G
ENST00000515320.5:c.498A>G	ENSP00000424613.1:p.Lys166=
NM_000414.3:c.552A>G	NP_000405.1:p.Lys184=
NM_001199291.2:c.627A>G	NP_001186220.1:p.Lys209=
NM_001199292.1:c.498A>G	NP_001186221.1:p.Lys166=
NM_001292027.1:c.480A>G	NP_001278956.1:p.Lys160=
NM_001292028.1:c.132A>G	NP_001278957.1:p.Lys44=
NM_000414.4:c.552A>G MANE Select	NP_000405.1:p.Lys184=
NM_001199291.3:c.627A>G	NP_001186220.1:p.Lys209=
NM_001199292.2:c.498A>G	NP_001186221.1:p.Lys166=
NM_001292027.2:c.480A>G	NP_001278956.1:p.Lys160=
NM_001292028.2:c.132A>G	NP_001278957.1:p.Lys44=
NM_001374497.1:c.543A>G	NP_001361426.1:p.Lys181=
NM_001374498.1:c.552A>G	NP_001361427.1:p.Lys184=
NM_001374499.1:c.225A>G	NP_001361428.1:p.Lys75=
NM_001374500.1:c.111A>G	NP_001361429.1:p.Lys37=
NM_001374501.1:c.141A>G	NP_001361430.1:p.Lys47=
NM_001374502.1:c.141A>G	NP_001361431.1:p.Lys47=
NM_001374503.1:c.141A>G	NP_001361432.1:p.Lys47=
NR_164653.1:n.631A>G
NR_164654.1:n.819A>G