Canonical Allele Identifier: CA360864963

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118811540T>G (hg19) ; chr5:g.119475845T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119475845T>G , CM000667.2:g.119475845T>G	GRCh38
NC_000005.9:g.118811540T>G , CM000667.1:g.118811540T>G	GRCh37
NC_000005.8:g.118839439T>G	NCBI36
NG_008182.1:g.28393T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.324T>G	ENSP00000426272.2:p.Phe108Leu
ENST00000518349.6:c.112+19477T>G	ENSP00000507185.1:n.112+19477T>G
ENST00000682445.1:c.*205T>G	ENSP00000508061.1:n.*205T>G
ENST00000682531.1:n.425T>G
ENST00000682626.1:c.377+118T>G	ENSP00000507857.1:n.377+118T>G
ENST00000682996.1:c.324T>G	ENSP00000507792.1:p.Phe108Leu
ENST00000683265.1:n.417T>G
ENST00000683371.1:c.*454T>G	ENSP00000508376.1:n.*454T>G
ENST00000683390.1:n.468T>G
ENST00000683936.1:c.*209T>G	ENSP00000507721.1:n.*209T>G
ENST00000683974.1:n.406T>G
ENST00000684160.1:c.399T>G	ENSP00000507821.1:p.Phe133Leu
ENST00000684214.1:c.324T>G	ENSP00000508071.1:p.Phe108Leu
ENST00000414835.7:c.399T>G	ENSP00000411960.3:p.Phe133Leu
ENST00000510025.7:c.324T>G MANE Select	ENSP00000424940.3:p.Phe108Leu
ENST00000643250.1:c.*205T>G	ENSP00000494737.1:n.*205T>G
ENST00000644146.1:c.324T>G	ENSP00000494808.1:p.Phe108Leu
ENST00000645832.1:c.*209T>G	ENSP00000494316.1:n.*209T>G
ENST00000646058.1:c.324T>G	ENSP00000493579.1:p.Phe108Leu
ENST00000646355.1:c.*330T>G	ENSP00000493801.1:n.*330T>G
ENST00000646554.1:c.*205T>G	ENSP00000494542.1:n.*205T>G
ENST00000646590.1:c.324T>G	ENSP00000494892.1:p.Phe108Leu
ENST00000647335.1:c.*291T>G	ENSP00000495180.1:n.*291T>G
ENST00000647342.1:c.*205T>G	ENSP00000494992.1:n.*205T>G
ENST00000256216.10:c.324T>G	ENSP00000256216.6:p.Phe108Leu
ENST00000414835.6:c.-88T>G	ENSP00000411960.2:n.-88T>G
ENST00000442060.7:c.324T>G	ENSP00000390208.3:p.Phe108Leu
ENST00000503168.5:n.313T>G
ENST00000504811.5:c.399T>G	ENSP00000420914.1:p.Phe133Leu
ENST00000507695.1:n.296T>G
ENST00000510025.5:c.252T>G	ENSP00000424940.1:p.Phe84Leu
ENST00000511186.5:n.455T>G
ENST00000512841.5:n.372T>G
ENST00000515235.6:n.384T>G
ENST00000515320.5:c.270T>G	ENSP00000424613.1:p.Phe90Leu
NM_000414.3:c.324T>G	NP_000405.1:p.Phe108Leu
NM_001199291.2:c.399T>G	NP_001186220.1:p.Phe133Leu
NM_001199292.1:c.270T>G	NP_001186221.1:p.Phe90Leu
NM_001292027.1:c.252T>G	NP_001278956.1:p.Phe84Leu
NM_001292028.1:c.-88T>G	NP_001278957.1:n.-88T>G
NM_000414.4:c.324T>G MANE Select	NP_000405.1:p.Phe108Leu
NM_001199291.3:c.399T>G	NP_001186220.1:p.Phe133Leu
NM_001199292.2:c.270T>G	NP_001186221.1:p.Phe90Leu
NM_001292027.2:c.252T>G	NP_001278956.1:p.Phe84Leu
NM_001292028.2:c.-88T>G	NP_001278957.1:n.-88T>G
NM_001374497.1:c.324T>G	NP_001361426.1:p.Phe108Leu
NM_001374498.1:c.324T>G	NP_001361427.1:p.Phe108Leu
NM_001374499.1:c.22+118T>G	NP_001361428.1:n.22+118T>G
NM_001374500.1:c.-215T>G	NP_001361429.1:n.-215T>G
NM_001374501.1:c.-88T>G	NP_001361430.1:n.-88T>G
NM_001374502.1:c.-88T>G	NP_001361431.1:n.-88T>G
NM_001374503.1:c.-88T>G	NP_001361432.1:n.-88T>G
NR_164653.1:n.403T>G
NR_164654.1:n.591T>G