Canonical Allele Identifier: CA2695201154

Gene: ACSF3

Linked Data

• ClinVar Variation Id: 2680592
• ClinVar RCV Id: RCV003466695

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145391dup , CM000678.2:g.89145391dup	GRCh38
NC_000016.9:g.89211799dup , CM000678.1:g.89211799dup	GRCh37
NC_000016.8:g.87739300dup	NCBI36
NG_031961.1:g.56583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1491dup	ENSP00000320646.4:p.Ser498GlnfsTer?
ENST00000614302.5:c.1491dup MANE Select	ENSP00000479130.1:p.Ser498GlnfsTer?
ENST00000649953.1:c.1701dup	ENSP00000497456.1:p.Ser568GlnfsTer?
ENST00000317447.8:c.1491dup	ENSP00000320646.4:p.Ser498GlnfsTer?
ENST00000378345.8:c.696dup	ENSP00000367596.4:p.Ser233GlnfsTer?
ENST00000406948.7:c.1491dup	ENSP00000384627.3:p.Ser498GlnfsTer?
ENST00000537116.5:n.617dup
ENST00000537155.1:n.231dup
ENST00000542688.5:c.*235dup	ENSP00000446281.1:n.*235dup
ENST00000544543.5:c.696dup	ENSP00000442781.1:p.Ser233GlnfsTer?
ENST00000562204.1:n.464dup
ENST00000614302.4:c.1491dup	ENSP00000479130.1:p.Ser498GlnfsTer?
NM_001127214.3:c.1491dup	NP_001120686.1:p.Ser498GlnfsTer?
NM_001243279.2:c.1491dup	NP_001230208.1:p.Ser498GlnfsTer?
NM_001284316.1:c.696dup	NP_001271245.1:p.Ser233GlnfsTer?
NM_174917.4:c.1491dup	NP_777577.2:p.Ser498GlnfsTer?
NR_045667.2:n.617dup
NR_104293.1:n.1925dup
XM_005256293.1:c.1491dup	XP_005256350.1:p.Ser498GlnfsTer?
XM_011522942.1:c.1491dup	XP_011521244.1:p.Ser498GlnfsTer?
XM_011522943.1:c.1491dup	XP_011521245.1:p.Ser498GlnfsTer?
XR_933239.1:n.1932dup
XR_933240.1:n.1929dup
XR_933241.1:n.1686dup
NR_147928.1:n.1969dup
NR_147929.1:n.1723dup
XM_005256293.2:c.1491dup	XP_005256350.1:p.Ser498GlnfsTer?
XM_017023018.1:c.1491dup	XP_016878507.1:p.Ser498GlnfsTer?
XM_017023019.1:c.1491dup	XP_016878508.1:p.Ser498GlnfsTer?
XM_017023020.2:c.-3614dup	XP_016878509.1:n.-3614dup
XM_017023022.1:c.624dup	XP_016878511.1:p.Ser209GlnfsTer?
XM_024450186.1:c.696dup	XP_024305954.1:p.Ser233GlnfsTer?
XM_024450187.1:c.696dup	XP_024305955.1:p.Ser233GlnfsTer?
XR_001751864.2:n.1738dup
XR_001751865.1:n.1685dup
XR_933240.3:n.1928dup
NM_001127214.4:c.1491dup	NP_001120686.1:p.Ser498GlnfsTer?
NM_001243279.3:c.1491dup MANE Select	NP_001230208.1:p.Ser498GlnfsTer?
NM_001284316.2:c.696dup	NP_001271245.1:p.Ser233GlnfsTer?
NM_174917.5:c.1491dup	NP_777577.2:p.Ser498GlnfsTer?
NR_104293.2:n.1882dup
NR_147928.2:n.1926dup
NR_147929.2:n.1680dup