Canonical Allele Identifier: CA2634920793

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89146056-C-CGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146056_89146057insGGGG , CM000678.2:g.89146056_89146057insGGGG	GRCh38
NC_000016.9:g.89212464_89212465insGGGG , CM000678.1:g.89212464_89212465insGGGG	GRCh37
NC_000016.8:g.87739965_87739966insGGGG	NCBI36
NG_031961.1:g.57248_57249insGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1613+7_1613+8insGGGG	ENSP00000320646.4:n.1613+7_1613+8insGGGG
ENST00000614302.5:c.1613+7_1613+8insGGGG MANE Select	ENSP00000479130.1:n.1613+7_1613+8insGGGG
ENST00000649953.1:c.1823+7_1823+8insGGGG	ENSP00000497456.1:n.1823+7_1823+8insGGGG
ENST00000317447.8:c.1613+7_1613+8insGGGG	ENSP00000320646.4:n.1613+7_1613+8insGGGG
ENST00000378345.8:c.818+7_818+8insGGGG	ENSP00000367596.4:n.818+7_818+8insGGGG
ENST00000406948.7:c.1613+7_1613+8insGGGG	ENSP00000384627.3:n.1613+7_1613+8insGGGG
ENST00000535176.1:c.100+7_100+8insGGGG
ENST00000537116.5:n.739+7_739+8insGGGG
ENST00000537155.1:n.353+7_353+8insGGGG
ENST00000542688.5:c.*357+7_*357+8insGGGG	ENSP00000446281.1:n.*357+7_*357+8insGGGG
ENST00000614302.4:c.1613+7_1613+8insGGGG	ENSP00000479130.1:n.1613+7_1613+8insGGGG
NM_001127214.3:c.1613+7_1613+8insGGGG	NP_001120686.1:n.1613+7_1613+8insGGGG
NM_001243279.2:c.1613+7_1613+8insGGGG	NP_001230208.1:n.1613+7_1613+8insGGGG
NM_001284316.1:c.818+7_818+8insGGGG	NP_001271245.1:n.818+7_818+8insGGGG
NM_174917.4:c.1613+7_1613+8insGGGG	NP_777577.2:n.1613+7_1613+8insGGGG
NR_045667.2:n.739+7_739+8insGGGG
NR_104293.1:n.2047+7_2047+8insGGGG
XM_005256293.1:c.1613+7_1613+8insGGGG	XP_005256350.1:n.1613+7_1613+8insGGGG
XM_011522942.1:c.1613+7_1613+8insGGGG	XP_011521244.1:n.1613+7_1613+8insGGGG
XM_011522943.1:c.1613+7_1613+8insGGGG	XP_011521245.1:n.1613+7_1613+8insGGGG
XR_933239.1:n.2054+7_2054+8insGGGG
XR_933240.1:n.2051+7_2051+8insGGGG
XR_933241.1:n.1808+7_1808+8insGGGG
NR_147928.1:n.2091+7_2091+8insGGGG
NR_147929.1:n.1845+7_1845+8insGGGG
XM_005256293.2:c.1613+7_1613+8insGGGG	XP_005256350.1:n.1613+7_1613+8insGGGG
XM_017023018.1:c.1613+7_1613+8insGGGG	XP_016878507.1:n.1613+7_1613+8insGGGG
XM_017023019.1:c.1613+7_1613+8insGGGG	XP_016878508.1:n.1613+7_1613+8insGGGG
XM_017023020.2:c.-3492+7_-3492+8insGGGG	XP_016878509.1:n.-3492+7_-3492+8insGGGG
XM_017023022.1:c.746+7_746+8insGGGG	XP_016878511.1:n.746+7_746+8insGGGG
XM_024450186.1:c.818+7_818+8insGGGG	XP_024305954.1:n.818+7_818+8insGGGG
XM_024450187.1:c.818+7_818+8insGGGG	XP_024305955.1:n.818+7_818+8insGGGG
XR_001751864.2:n.1860+7_1860+8insGGGG
XR_001751865.1:n.1807+7_1807+8insGGGG
XR_933240.3:n.2050+7_2050+8insGGGG
NM_001127214.4:c.1613+7_1613+8insGGGG	NP_001120686.1:n.1613+7_1613+8insGGGG
NM_001243279.3:c.1613+7_1613+8insGGGG MANE Select	NP_001230208.1:n.1613+7_1613+8insGGGG
NM_001284316.2:c.818+7_818+8insGGGG	NP_001271245.1:n.818+7_818+8insGGGG
NM_174917.5:c.1613+7_1613+8insGGGG	NP_777577.2:n.1613+7_1613+8insGGGG
NR_104293.2:n.2004+7_2004+8insGGGG
NR_147928.2:n.2048+7_2048+8insGGGG
NR_147929.2:n.1802+7_1802+8insGGGG