Canonical Allele Identifier: CA360866194

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118814590G>T (hg19) ; chr5:g.119478895G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119478895G>T , CM000667.2:g.119478895G>T	GRCh38
NC_000005.9:g.118814590G>T , CM000667.1:g.118814590G>T	GRCh37
NC_000005.8:g.118842489G>T	NCBI36
NG_008182.1:g.31443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.496G>T	ENSP00000426272.2:p.Ala166Ser
ENST00000518349.6:c.113-17648G>T	ENSP00000507185.1:n.113-17648G>T
ENST00000682445.1:c.*377G>T	ENSP00000508061.1:n.*377G>T
ENST00000682531.1:n.597G>T
ENST00000682626.1:c.*2G>T	ENSP00000507857.1:n.*2G>T
ENST00000682996.1:c.496G>T	ENSP00000507792.1:p.Ala166Ser
ENST00000683265.1:n.589G>T
ENST00000683371.1:c.*626G>T	ENSP00000508376.1:n.*626G>T
ENST00000683390.1:n.2186G>T
ENST00000683549.1:n.417G>T
ENST00000683936.1:c.*381G>T	ENSP00000507721.1:n.*381G>T
ENST00000683974.1:n.578G>T
ENST00000683996.1:c.85G>T	ENSP00000507060.1:p.Ala29Ser
ENST00000684131.1:n.335G>T
ENST00000684160.1:c.*186G>T	ENSP00000507821.1:n.*186G>T
ENST00000684214.1:c.496G>T	ENSP00000508071.1:p.Ala166Ser
ENST00000414835.7:c.571G>T	ENSP00000411960.3:p.Ala191Ser
ENST00000510025.7:c.496G>T MANE Select	ENSP00000424940.3:p.Ala166Ser
ENST00000643250.1:c.*368G>T	ENSP00000494737.1:n.*368G>T
ENST00000644146.1:c.*74G>T	ENSP00000494808.1:n.*74G>T
ENST00000645099.1:c.55G>T	ENSP00000496091.1:p.Ala19Ser
ENST00000645702.1:c.85G>T	ENSP00000496432.1:p.Ala29Ser
ENST00000645832.1:c.*381G>T	ENSP00000494316.1:n.*381G>T
ENST00000646058.1:c.496G>T	ENSP00000493579.1:p.Ala166Ser
ENST00000646355.1:c.*502G>T	ENSP00000493801.1:n.*502G>T
ENST00000646554.1:c.*474G>T	ENSP00000494542.1:n.*474G>T
ENST00000646590.1:c.487G>T	ENSP00000494892.1:p.Ala163Ser
ENST00000647335.1:c.*463G>T	ENSP00000495180.1:n.*463G>T
ENST00000647342.1:c.*427G>T	ENSP00000494992.1:n.*427G>T
ENST00000256216.10:c.496G>T	ENSP00000256216.6:p.Ala166Ser
ENST00000414835.6:c.76G>T	ENSP00000411960.2:p.Ala26Ser
ENST00000442060.7:c.496G>T	ENSP00000390208.3:p.Ala166Ser
ENST00000503168.5:n.485G>T
ENST00000504811.5:c.571G>T	ENSP00000420914.1:p.Ala191Ser
ENST00000505181.5:n.199G>T
ENST00000508788.5:n.398G>T
ENST00000509514.5:c.-389G>T	ENSP00000426272.1:n.-389G>T
ENST00000510025.5:c.424G>T	ENSP00000424940.1:p.Ala142Ser
ENST00000512644.1:n.64G>T
ENST00000512841.5:n.544G>T
ENST00000513628.5:c.85G>T	ENSP00000425993.1:p.Ala29Ser
ENST00000515235.6:n.556G>T
ENST00000515320.5:c.442G>T	ENSP00000424613.1:p.Ala148Ser
NM_000414.3:c.496G>T	NP_000405.1:p.Ala166Ser
NM_001199291.2:c.571G>T	NP_001186220.1:p.Ala191Ser
NM_001199292.1:c.442G>T	NP_001186221.1:p.Ala148Ser
NM_001292027.1:c.424G>T	NP_001278956.1:p.Ala142Ser
NM_001292028.1:c.76G>T	NP_001278957.1:p.Ala26Ser
NM_000414.4:c.496G>T MANE Select	NP_000405.1:p.Ala166Ser
NM_001199291.3:c.571G>T	NP_001186220.1:p.Ala191Ser
NM_001199292.2:c.442G>T	NP_001186221.1:p.Ala148Ser
NM_001292027.2:c.424G>T	NP_001278956.1:p.Ala142Ser
NM_001292028.2:c.76G>T	NP_001278957.1:p.Ala26Ser
NM_001374497.1:c.487G>T	NP_001361426.1:p.Ala163Ser
NM_001374498.1:c.496G>T	NP_001361427.1:p.Ala166Ser
NM_001374499.1:c.169G>T	NP_001361428.1:p.Ala57Ser
NM_001374500.1:c.55G>T	NP_001361429.1:p.Ala19Ser
NM_001374501.1:c.85G>T	NP_001361430.1:p.Ala29Ser
NM_001374502.1:c.85G>T	NP_001361431.1:p.Ala29Ser
NM_001374503.1:c.85G>T	NP_001361432.1:p.Ala29Ser
NR_164653.1:n.575G>T
NR_164654.1:n.763G>T