Canonical Allele Identifier: CA360864876

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118811407T>C (hg19) ; chr5:g.119475712T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119475712T>C , CM000667.2:g.119475712T>C	GRCh38
NC_000005.9:g.118811407T>C , CM000667.1:g.118811407T>C	GRCh37
NC_000005.8:g.118839306T>C	NCBI36
NG_008182.1:g.28260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.287T>C	ENSP00000426272.2:p.Val96Ala
ENST00000518349.6:c.112+19344T>C	ENSP00000507185.1:n.112+19344T>C
ENST00000682445.1:c.*168T>C	ENSP00000508061.1:n.*168T>C
ENST00000682531.1:n.388T>C
ENST00000682626.1:c.362T>C	ENSP00000507857.1:p.Val121Ala
ENST00000682996.1:c.287T>C	ENSP00000507792.1:p.Val96Ala
ENST00000683265.1:n.380T>C
ENST00000683371.1:c.*417T>C	ENSP00000508376.1:n.*417T>C
ENST00000683390.1:n.335T>C
ENST00000683936.1:c.*172T>C	ENSP00000507721.1:n.*172T>C
ENST00000683974.1:n.369T>C
ENST00000684160.1:c.362T>C	ENSP00000507821.1:p.Val121Ala
ENST00000684214.1:c.287T>C	ENSP00000508071.1:p.Val96Ala
ENST00000414835.7:c.362T>C	ENSP00000411960.3:p.Val121Ala
ENST00000510025.7:c.287T>C MANE Select	ENSP00000424940.3:p.Val96Ala
ENST00000643250.1:c.*168T>C	ENSP00000494737.1:n.*168T>C
ENST00000644146.1:c.287T>C	ENSP00000494808.1:p.Val96Ala
ENST00000645832.1:c.*172T>C	ENSP00000494316.1:n.*172T>C
ENST00000646058.1:c.287T>C	ENSP00000493579.1:p.Val96Ala
ENST00000646355.1:c.*293T>C	ENSP00000493801.1:n.*293T>C
ENST00000646554.1:c.*168T>C	ENSP00000494542.1:n.*168T>C
ENST00000646590.1:c.287T>C	ENSP00000494892.1:p.Val96Ala
ENST00000647335.1:c.*254T>C	ENSP00000495180.1:n.*254T>C
ENST00000647342.1:c.*168T>C	ENSP00000494992.1:n.*168T>C
ENST00000256216.10:c.287T>C	ENSP00000256216.6:p.Val96Ala
ENST00000414835.6:c.-125T>C	ENSP00000411960.2:n.-125T>C
ENST00000442060.7:c.287T>C	ENSP00000390208.3:p.Val96Ala
ENST00000503168.5:n.276T>C
ENST00000504811.5:c.362T>C	ENSP00000420914.1:p.Val121Ala
ENST00000507695.1:n.259T>C
ENST00000510025.5:c.215T>C	ENSP00000424940.1:p.Val72Ala
ENST00000511186.5:n.418T>C
ENST00000512841.5:n.335T>C
ENST00000515235.6:n.347T>C
ENST00000515320.5:c.233T>C	ENSP00000424613.1:p.Val78Ala
NM_000414.3:c.287T>C	NP_000405.1:p.Val96Ala
NM_001199291.2:c.362T>C	NP_001186220.1:p.Val121Ala
NM_001199292.1:c.233T>C	NP_001186221.1:p.Val78Ala
NM_001292027.1:c.215T>C	NP_001278956.1:p.Val72Ala
NM_001292028.1:c.-125T>C	NP_001278957.1:n.-125T>C
NM_000414.4:c.287T>C MANE Select	NP_000405.1:p.Val96Ala
NM_001199291.3:c.362T>C	NP_001186220.1:p.Val121Ala
NM_001199292.2:c.233T>C	NP_001186221.1:p.Val78Ala
NM_001292027.2:c.215T>C	NP_001278956.1:p.Val72Ala
NM_001292028.2:c.-125T>C	NP_001278957.1:n.-125T>C
NM_001374497.1:c.287T>C	NP_001361426.1:p.Val96Ala
NM_001374498.1:c.287T>C	NP_001361427.1:p.Val96Ala
NM_001374499.1:c.7T>C	NP_001361428.1:p.Trp3Arg
NM_001374500.1:c.-252T>C	NP_001361429.1:n.-252T>C
NM_001374501.1:c.-125T>C	NP_001361430.1:n.-125T>C
NM_001374502.1:c.-125T>C	NP_001361431.1:n.-125T>C
NM_001374503.1:c.-125T>C	NP_001361432.1:n.-125T>C
NR_164653.1:n.366T>C
NR_164654.1:n.554T>C