Canonical Allele Identifier: CA645586740

Gene: ACSF3

Linked Data

• COSMIC: COSM5833208

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145312_89145313del , CM000678.2:g.89145312_89145313del	GRCh38
NC_000016.9:g.89211720_89211721del , CM000678.1:g.89211720_89211721del	GRCh37
NC_000016.8:g.87739221_87739222del	NCBI36
NG_031961.1:g.56504_56505del

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1412_1413del	ENSP00000320646.4:p.Arg471HisfsTer?
ENST00000614302.5:c.1412_1413del MANE Select	ENSP00000479130.1:p.Arg471HisfsTer?
ENST00000649953.1:c.1622_1623del	ENSP00000497456.1:p.Arg541HisfsTer?
ENST00000317447.8:c.1412_1413del	ENSP00000320646.4:p.Arg471HisfsTer?
ENST00000378345.8:c.617_618del	ENSP00000367596.4:p.Arg206HisfsTer?
ENST00000406948.7:c.1412_1413del	ENSP00000384627.3:p.Arg471HisfsTer?
ENST00000537116.5:n.538_539del
ENST00000537155.1:n.152_153del
ENST00000542688.5:c.*156_*157del	ENSP00000446281.1:n.*156_*157del
ENST00000544543.5:c.617_618del	ENSP00000442781.1:p.Arg206HisfsTer?
ENST00000562204.1:n.385_386del
ENST00000614302.4:c.1412_1413del	ENSP00000479130.1:p.Arg471HisfsTer?
NM_001127214.3:c.1412_1413del	NP_001120686.1:p.Arg471HisfsTer?
NM_001243279.2:c.1412_1413del	NP_001230208.1:p.Arg471HisfsTer?
NM_001284316.1:c.617_618del	NP_001271245.1:p.Arg206HisfsTer?
NM_174917.4:c.1412_1413del	NP_777577.2:p.Arg471HisfsTer?
NR_045667.2:n.538_539del
NR_104293.1:n.1846_1847del
XM_005256293.1:c.1412_1413del	XP_005256350.1:p.Arg471HisfsTer?
XM_011522942.1:c.1412_1413del	XP_011521244.1:p.Arg471HisfsTer?
XM_011522943.1:c.1412_1413del	XP_011521245.1:p.Arg471HisfsTer?
XR_933239.1:n.1853_1854del
XR_933240.1:n.1850_1851del
XR_933241.1:n.1607_1608del
NR_147928.1:n.1890_1891del
NR_147929.1:n.1644_1645del
XM_005256293.2:c.1412_1413del	XP_005256350.1:p.Arg471HisfsTer?
XM_017023018.1:c.1412_1413del	XP_016878507.1:p.Arg471HisfsTer?
XM_017023019.1:c.1412_1413del	XP_016878508.1:p.Arg471HisfsTer?
XM_017023020.2:c.-3693_-3692del	XP_016878509.1:n.-3693_-3692del
XM_017023022.1:c.545_546del	XP_016878511.1:p.Arg182HisfsTer?
XM_024450186.1:c.617_618del	XP_024305954.1:p.Arg206HisfsTer?
XM_024450187.1:c.617_618del	XP_024305955.1:p.Arg206HisfsTer?
XR_001751864.2:n.1659_1660del
XR_001751865.1:n.1606_1607del
XR_933240.3:n.1849_1850del
NM_001127214.4:c.1412_1413del	NP_001120686.1:p.Arg471HisfsTer?
NM_001243279.3:c.1412_1413del MANE Select	NP_001230208.1:p.Arg471HisfsTer?
NM_001284316.2:c.617_618del	NP_001271245.1:p.Arg206HisfsTer?
NM_174917.5:c.1412_1413del	NP_777577.2:p.Arg471HisfsTer?
NR_104293.2:n.1803_1804del
NR_147928.2:n.1847_1848del
NR_147929.2:n.1601_1602del