Canonical Allele Identifier: CA1577038551

Gene: HSD17B4

Linked Data

• dbSNP Id: rs1752477032
• gnomAD v4: 5-119514902-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119514902G>C , CM000667.2:g.119514902G>C	GRCh38
NC_000005.9:g.118850597G>C , CM000667.1:g.118850597G>C	GRCh37
NC_000005.8:g.118878496G>C	NCBI36
NG_008182.1:g.67450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.1369-79G>C	ENSP00000426272.2:n.1369-79G>C
ENST00000518349.6:c.682-79G>C	ENSP00000507185.1:n.682-79G>C
ENST00000520244.6:n.3097G>C
ENST00000682445.1:c.*1319-79G>C	ENSP00000508061.1:n.*1319-79G>C
ENST00000682531.1:n.3330-79G>C
ENST00000682626.1:c.*944-79G>C	ENSP00000507857.1:n.*944-79G>C
ENST00000682996.1:c.1366-79G>C	ENSP00000507792.1:n.1366-79G>C
ENST00000683265.1:n.3224-79G>C
ENST00000683335.1:n.2761G>C
ENST00000683371.1:c.*1568-79G>C	ENSP00000508376.1:n.*1568-79G>C
ENST00000683372.1:n.3448-79G>C
ENST00000683390.1:n.3128-79G>C
ENST00000683549.1:n.3052-79G>C
ENST00000683936.1:c.*3016-79G>C	ENSP00000507721.1:n.*3016-79G>C
ENST00000683974.1:n.3213-125G>C
ENST00000683996.1:c.*648-79G>C	ENSP00000507060.1:n.*648-79G>C
ENST00000684131.1:n.2970-79G>C
ENST00000684160.1:c.*1128-79G>C	ENSP00000507821.1:n.*1128-79G>C
ENST00000684214.1:c.1438-79G>C	ENSP00000508071.1:n.1438-79G>C
ENST00000414835.7:c.1513-79G>C	ENSP00000411960.3:n.1513-79G>C
ENST00000510025.7:c.1438-79G>C MANE Select	ENSP00000424940.3:n.1438-79G>C
ENST00000643250.1:c.*1310-79G>C	ENSP00000494737.1:n.*1310-79G>C
ENST00000644146.1:c.*2709-79G>C	ENSP00000494808.1:n.*2709-79G>C
ENST00000645099.1:c.997-79G>C	ENSP00000496091.1:n.997-79G>C
ENST00000645702.1:c.*841-79G>C	ENSP00000496432.1:n.*841-79G>C
ENST00000645832.1:c.*1323-79G>C	ENSP00000494316.1:n.*1323-79G>C
ENST00000646058.1:c.1438-79G>C	ENSP00000493579.1:n.1438-79G>C
ENST00000646355.1:c.*1444-79G>C	ENSP00000493801.1:n.*1444-79G>C
ENST00000646554.1:c.*1416-79G>C	ENSP00000494542.1:n.*1416-79G>C
ENST00000647335.1:c.*1405-79G>C	ENSP00000495180.1:n.*1405-79G>C
ENST00000647342.1:c.*1369-79G>C	ENSP00000494992.1:n.*1369-79G>C
ENST00000256216.10:c.1438-79G>C	ENSP00000256216.6:n.1438-79G>C
ENST00000414835.6:c.1018-79G>C	ENSP00000411960.2:n.1018-79G>C
ENST00000442060.7:c.1503-79G>C	ENSP00000390208.3:n.1503-79G>C
ENST00000504811.5:c.1513-79G>C	ENSP00000420914.1:n.1513-79G>C
ENST00000509514.5:c.652-79G>C	ENSP00000426272.1:n.652-79G>C
ENST00000510025.5:c.1366-79G>C	ENSP00000424940.1:n.1366-79G>C
ENST00000513628.5:c.1027-79G>C	ENSP00000425993.1:n.1027-79G>C
ENST00000515235.6:n.3191-79G>C
ENST00000515320.5:c.1384-79G>C	ENSP00000424613.1:n.1384-79G>C
ENST00000518349.5:n.572-79G>C
ENST00000520244.5:n.221-79G>C
ENST00000522415.5:n.105-79G>C
NM_000414.3:c.1438-79G>C	NP_000405.1:n.1438-79G>C
NM_001199291.2:c.1513-79G>C	NP_001186220.1:n.1513-79G>C
NM_001199292.1:c.1384-79G>C	NP_001186221.1:n.1384-79G>C
NM_001292027.1:c.1366-79G>C	NP_001278956.1:n.1366-79G>C
NM_001292028.1:c.1018-79G>C	NP_001278957.1:n.1018-79G>C
NM_000414.4:c.1438-79G>C MANE Select	NP_000405.1:n.1438-79G>C
NM_001199291.3:c.1513-79G>C	NP_001186220.1:n.1513-79G>C
NM_001199292.2:c.1384-79G>C	NP_001186221.1:n.1384-79G>C
NM_001292027.2:c.1366-79G>C	NP_001278956.1:n.1366-79G>C
NM_001292028.2:c.1018-79G>C	NP_001278957.1:n.1018-79G>C
NM_001374497.1:c.1429-79G>C	NP_001361426.1:n.1429-79G>C
NM_001374498.1:c.1366-79G>C	NP_001361427.1:n.1366-79G>C
NM_001374499.1:c.1111-79G>C	NP_001361428.1:n.1111-79G>C
NM_001374500.1:c.997-79G>C	NP_001361429.1:n.997-79G>C
NM_001374501.1:c.1027-79G>C	NP_001361430.1:n.1027-79G>C
NM_001374502.1:c.1027-79G>C	NP_001361431.1:n.1027-79G>C
NM_001374503.1:c.1027-79G>C	NP_001361432.1:n.1027-79G>C
NR_164653.1:n.1535-79G>C
NR_164654.1:n.1803-79G>C