Canonical Allele Identifier: CA360871117

Gene: HSD17B4

Linked Data

• MyVariant Identifiers: chr5:g.118867019T>A (hg19) ; chr5:g.119531324T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119531324T>A , CM000667.2:g.119531324T>A	GRCh38
NC_000005.9:g.118867019T>A , CM000667.1:g.118867019T>A	GRCh37
NC_000005.8:g.118894918T>A	NCBI36
NG_008182.1:g.83872T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000509514.6:c.1844T>A	ENSP00000426272.2:p.Ile615Asn
ENST00000518349.6:c.1157T>A	ENSP00000507185.1:p.Ile386Asn
ENST00000682445.1:c.*1794T>A	ENSP00000508061.1:n.*1794T>A
ENST00000682531.1:n.3805T>A
ENST00000682626.1:c.*1419T>A	ENSP00000507857.1:n.*1419T>A
ENST00000682996.1:c.1841T>A	ENSP00000507792.1:p.Ile614Asn
ENST00000683265.1:n.3699T>A
ENST00000683335.1:n.3315T>A
ENST00000683371.1:c.*2043T>A	ENSP00000508376.1:n.*2043T>A
ENST00000683372.1:n.3923T>A
ENST00000683390.1:n.3603T>A
ENST00000683476.1:n.755T>A
ENST00000683549.1:n.3527T>A
ENST00000683936.1:c.*3491T>A	ENSP00000507721.1:n.*3491T>A
ENST00000683974.1:n.3642T>A
ENST00000683996.1:c.*1123T>A	ENSP00000507060.1:n.*1123T>A
ENST00000684131.1:n.3445T>A
ENST00000684160.1:c.*1603T>A	ENSP00000507821.1:n.*1603T>A
ENST00000684214.1:c.1854+1344T>A	ENSP00000508071.1:n.1854+1344T>A
ENST00000414835.7:c.1988T>A	ENSP00000411960.3:p.Ile663Asn
ENST00000510025.7:c.1913T>A MANE Select	ENSP00000424940.3:p.Ile638Asn
ENST00000643250.1:c.*1785T>A	ENSP00000494737.1:n.*1785T>A
ENST00000644146.1:c.*3184T>A	ENSP00000494808.1:n.*3184T>A
ENST00000645099.1:c.1472T>A	ENSP00000496091.1:p.Ile491Asn
ENST00000645702.1:c.*1316T>A	ENSP00000496432.1:n.*1316T>A
ENST00000645832.1:c.*1798T>A	ENSP00000494316.1:n.*1798T>A
ENST00000646058.1:c.1913T>A	ENSP00000493579.1:p.Ile638Asn
ENST00000646355.1:c.*1919T>A	ENSP00000493801.1:n.*1919T>A
ENST00000646554.1:c.*1891T>A	ENSP00000494542.1:n.*1891T>A
ENST00000647335.1:c.*1880T>A	ENSP00000495180.1:n.*1880T>A
ENST00000647342.1:c.*1844T>A	ENSP00000494992.1:n.*1844T>A
ENST00000256216.10:c.1913T>A	ENSP00000256216.6:p.Ile638Asn
ENST00000414835.6:c.1493T>A	ENSP00000411960.2:p.Ile498Asn
ENST00000442060.7:c.*468T>A	ENSP00000390208.3:n.*468T>A
ENST00000504811.5:c.1988T>A	ENSP00000420914.1:p.Ile663Asn
ENST00000509514.5:c.1127T>A	ENSP00000426272.1:p.Ile376Asn
ENST00000509606.1:n.208T>A
ENST00000509951.5:n.309+1344T>A
ENST00000510025.5:c.1841T>A	ENSP00000424940.1:p.Ile614Asn
ENST00000513628.5:c.1502T>A	ENSP00000425993.1:p.Ile501Asn
ENST00000515235.6:n.3666T>A
ENST00000515320.5:c.1859T>A	ENSP00000424613.1:p.Ile620Asn
ENST00000522415.5:n.580T>A
NM_000414.3:c.1913T>A	NP_000405.1:p.Ile638Asn
NM_001199291.2:c.1988T>A	NP_001186220.1:p.Ile663Asn
NM_001199292.1:c.1859T>A	NP_001186221.1:p.Ile620Asn
NM_001292027.1:c.1841T>A	NP_001278956.1:p.Ile614Asn
NM_001292028.1:c.1493T>A	NP_001278957.1:p.Ile498Asn
NM_000414.4:c.1913T>A MANE Select	NP_000405.1:p.Ile638Asn
NM_001199291.3:c.1988T>A	NP_001186220.1:p.Ile663Asn
NM_001199292.2:c.1859T>A	NP_001186221.1:p.Ile620Asn
NM_001292027.2:c.1841T>A	NP_001278956.1:p.Ile614Asn
NM_001292028.2:c.1493T>A	NP_001278957.1:p.Ile498Asn
NM_001374497.1:c.1904T>A	NP_001361426.1:p.Ile635Asn
NM_001374498.1:c.1841T>A	NP_001361427.1:p.Ile614Asn
NM_001374499.1:c.1586T>A	NP_001361428.1:p.Ile529Asn
NM_001374500.1:c.1472T>A	NP_001361429.1:p.Ile491Asn
NM_001374501.1:c.1502T>A	NP_001361430.1:p.Ile501Asn
NM_001374502.1:c.1502T>A	NP_001361431.1:p.Ile501Asn
NM_001374503.1:c.1502T>A	NP_001361432.1:p.Ile501Asn
NR_164653.1:n.2010T>A
NR_164654.1:n.2278T>A