Canonical Allele Identifier: CA2634920779

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89146048-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146050dup , CM000678.2:g.89146050dup	GRCh38
NC_000016.9:g.89212458dup , CM000678.1:g.89212458dup	GRCh37
NC_000016.8:g.87739959dup	NCBI36
NG_031961.1:g.57242dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1613+1dup
ENST00000614302.5:c.1613+1dup
ENST00000649953.1:c.1823+1dup
ENST00000317447.8:c.1613+1dup
ENST00000378345.8:c.818+1dup
ENST00000406948.7:c.1613+1dup
ENST00000535176.1:c.100+1dup
ENST00000537116.5:n.739+1dup
ENST00000537155.1:n.353+1dup
ENST00000542688.5:c.*357+1dup
ENST00000614302.4:c.1613+1dup
NM_001127214.3:c.1613+1dup
NM_001243279.2:c.1613+1dup
NM_001284316.1:c.818+1dup
NM_174917.4:c.1613+1dup
NR_045667.2:n.739+1dup
NR_104293.1:n.2047+1dup
XM_005256293.1:c.1613+1dup
XM_011522942.1:c.1613+1dup
XM_011522943.1:c.1613+1dup
XR_933239.1:n.2054+1dup
XR_933240.1:n.2051+1dup
XR_933241.1:n.1808+1dup
NR_147928.1:n.2091+1dup
NR_147929.1:n.1845+1dup
XM_005256293.2:c.1613+1dup
XM_017023018.1:c.1613+1dup
XM_017023019.1:c.1613+1dup
XM_017023020.2:c.-3492+1dup
XM_017023022.1:c.746+1dup
XM_024450186.1:c.818+1dup
XM_024450187.1:c.818+1dup
XR_001751864.2:n.1860+1dup
XR_001751865.1:n.1807+1dup
XR_933240.3:n.2050+1dup
NM_001127214.4:c.1613+1dup
NM_001243279.3:c.1613+1dup
NM_001284316.2:c.818+1dup
NM_174917.5:c.1613+1dup
NR_104293.2:n.2004+1dup
NR_147928.2:n.2048+1dup
NR_147929.2:n.1802+1dup