Canonical Allele Identifier: CA2674980160

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119489181-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119489181C>T , CM000667.2:g.119489181C>T	GRCh38
NC_000005.9:g.118824876C>T , CM000667.1:g.118824876C>T	GRCh37
NC_000005.8:g.118852775C>T	NCBI36
NG_008182.1:g.41729C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000509514.6:c.623-11C>T	ENSP00000426272.2:n.623-11C>T
ENST00000518349.6:c.113-7362C>T	ENSP00000507185.1:n.113-7362C>T
ENST00000682445.1:c.*504-11C>T	ENSP00000508061.1:n.*504-11C>T
ENST00000682531.1:n.724-11C>T
ENST00000682626.1:c.*129-11C>T	ENSP00000507857.1:n.*129-11C>T
ENST00000682996.1:c.623-11C>T	ENSP00000507792.1:n.623-11C>T
ENST00000683265.1:n.716-11C>T
ENST00000683371.1:c.*753-11C>T	ENSP00000508376.1:n.*753-11C>T
ENST00000683390.1:n.2313-11C>T
ENST00000683549.1:n.544-11C>T
ENST00000683936.1:c.*508-11C>T	ENSP00000507721.1:n.*508-11C>T
ENST00000683974.1:n.705-11C>T
ENST00000683996.1:c.212-11C>T	ENSP00000507060.1:n.212-11C>T
ENST00000684131.1:n.462-11C>T
ENST00000684160.1:c.*313-11C>T	ENSP00000507821.1:n.*313-11C>T
ENST00000684214.1:c.623-11C>T	ENSP00000508071.1:n.623-11C>T
ENST00000414835.7:c.698-11C>T	ENSP00000411960.3:n.698-11C>T
ENST00000510025.7:c.623-11C>T MANE Select	ENSP00000424940.3:n.623-11C>T
ENST00000643250.1:c.*495-11C>T	ENSP00000494737.1:n.*495-11C>T
ENST00000644146.1:c.*201-11C>T	ENSP00000494808.1:n.*201-11C>T
ENST00000645099.1:c.182-11C>T	ENSP00000496091.1:n.182-11C>T
ENST00000645702.1:c.*26-11C>T	ENSP00000496432.1:n.*26-11C>T
ENST00000645832.1:c.*508-11C>T	ENSP00000494316.1:n.*508-11C>T
ENST00000646058.1:c.623-11C>T	ENSP00000493579.1:n.623-11C>T
ENST00000646355.1:c.*629-11C>T	ENSP00000493801.1:n.*629-11C>T
ENST00000646554.1:c.*601-11C>T	ENSP00000494542.1:n.*601-11C>T
ENST00000647335.1:c.*590-11C>T	ENSP00000495180.1:n.*590-11C>T
ENST00000647342.1:c.*554-11C>T	ENSP00000494992.1:n.*554-11C>T
ENST00000256216.10:c.623-11C>T	ENSP00000256216.6:n.623-11C>T
ENST00000414835.6:c.203-11C>T	ENSP00000411960.2:n.203-11C>T
ENST00000442060.7:c.623-11C>T	ENSP00000390208.3:n.623-11C>T
ENST00000504811.5:c.698-11C>T	ENSP00000420914.1:n.698-11C>T
ENST00000505181.5:n.326-11C>T
ENST00000509514.5:c.-262-11C>T	ENSP00000426272.1:n.-262-11C>T
ENST00000510025.5:c.551-11C>T	ENSP00000424940.1:n.551-11C>T
ENST00000512644.1:n.191-11C>T
ENST00000513628.5:c.212-11C>T	ENSP00000425993.1:n.212-11C>T
ENST00000515235.6:n.683-11C>T
ENST00000515320.5:c.569-11C>T	ENSP00000424613.1:n.569-11C>T
NM_000414.3:c.623-11C>T	NP_000405.1:n.623-11C>T
NM_001199291.2:c.698-11C>T	NP_001186220.1:n.698-11C>T
NM_001199292.1:c.569-11C>T	NP_001186221.1:n.569-11C>T
NM_001292027.1:c.551-11C>T	NP_001278956.1:n.551-11C>T
NM_001292028.1:c.203-11C>T	NP_001278957.1:n.203-11C>T
NM_000414.4:c.623-11C>T MANE Select	NP_000405.1:n.623-11C>T
NM_001199291.3:c.698-11C>T	NP_001186220.1:n.698-11C>T
NM_001199292.2:c.569-11C>T	NP_001186221.1:n.569-11C>T
NM_001292027.2:c.551-11C>T	NP_001278956.1:n.551-11C>T
NM_001292028.2:c.203-11C>T	NP_001278957.1:n.203-11C>T
NM_001374497.1:c.614-11C>T	NP_001361426.1:n.614-11C>T
NM_001374498.1:c.623-11C>T	NP_001361427.1:n.623-11C>T
NM_001374499.1:c.296-11C>T	NP_001361428.1:n.296-11C>T
NM_001374500.1:c.182-11C>T	NP_001361429.1:n.182-11C>T
NM_001374501.1:c.212-11C>T	NP_001361430.1:n.212-11C>T
NM_001374502.1:c.212-11C>T	NP_001361431.1:n.212-11C>T
NM_001374503.1:c.212-11C>T	NP_001361432.1:n.212-11C>T
NR_164653.1:n.702-11C>T
NR_164654.1:n.890-11C>T