Canonical Allele Identifier: CA2634920803

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89146057-T-TGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146060_89146061insGGGGG , CM000678.2:g.89146060_89146061insGGGGG	GRCh38
NC_000016.9:g.89212468_89212469insGGGGG , CM000678.1:g.89212468_89212469insGGGGG	GRCh37
NC_000016.8:g.87739969_87739970insGGGGG	NCBI36
NG_031961.1:g.57252_57253insGGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1613+11_1613+12insGGGGG	ENSP00000320646.4:n.1613+11_1613+12insGGGGG
ENST00000614302.5:c.1613+11_1613+12insGGGGG MANE Select	ENSP00000479130.1:n.1613+11_1613+12insGGGGG
ENST00000649953.1:c.1823+11_1823+12insGGGGG	ENSP00000497456.1:n.1823+11_1823+12insGGGGG
ENST00000317447.8:c.1613+11_1613+12insGGGGG	ENSP00000320646.4:n.1613+11_1613+12insGGGGG
ENST00000378345.8:c.818+11_818+12insGGGGG	ENSP00000367596.4:n.818+11_818+12insGGGGG
ENST00000406948.7:c.1613+11_1613+12insGGGGG	ENSP00000384627.3:n.1613+11_1613+12insGGGGG
ENST00000535176.1:c.100+11_100+12insGGGGG
ENST00000537116.5:n.739+11_739+12insGGGGG
ENST00000537155.1:n.353+11_353+12insGGGGG
ENST00000542688.5:c.*357+11_*357+12insGGGGG	ENSP00000446281.1:n.*357+11_*357+12insGGGGG
ENST00000614302.4:c.1613+11_1613+12insGGGGG	ENSP00000479130.1:n.1613+11_1613+12insGGGGG
NM_001127214.3:c.1613+11_1613+12insGGGGG	NP_001120686.1:n.1613+11_1613+12insGGGGG
NM_001243279.2:c.1613+11_1613+12insGGGGG	NP_001230208.1:n.1613+11_1613+12insGGGGG
NM_001284316.1:c.818+11_818+12insGGGGG	NP_001271245.1:n.818+11_818+12insGGGGG
NM_174917.4:c.1613+11_1613+12insGGGGG	NP_777577.2:n.1613+11_1613+12insGGGGG
NR_045667.2:n.739+11_739+12insGGGGG
NR_104293.1:n.2047+11_2047+12insGGGGG
XM_005256293.1:c.1613+11_1613+12insGGGGG	XP_005256350.1:n.1613+11_1613+12insGGGGG
XM_011522942.1:c.1613+11_1613+12insGGGGG	XP_011521244.1:n.1613+11_1613+12insGGGGG
XM_011522943.1:c.1613+11_1613+12insGGGGG	XP_011521245.1:n.1613+11_1613+12insGGGGG
XR_933239.1:n.2054+11_2054+12insGGGGG
XR_933240.1:n.2051+11_2051+12insGGGGG
XR_933241.1:n.1808+11_1808+12insGGGGG
NR_147928.1:n.2091+11_2091+12insGGGGG
NR_147929.1:n.1845+11_1845+12insGGGGG
XM_005256293.2:c.1613+11_1613+12insGGGGG	XP_005256350.1:n.1613+11_1613+12insGGGGG
XM_017023018.1:c.1613+11_1613+12insGGGGG	XP_016878507.1:n.1613+11_1613+12insGGGGG
XM_017023019.1:c.1613+11_1613+12insGGGGG	XP_016878508.1:n.1613+11_1613+12insGGGGG
XM_017023020.2:c.-3492+11_-3492+12insGGGGG	XP_016878509.1:n.-3492+11_-3492+12insGGGGG
XM_017023022.1:c.746+11_746+12insGGGGG	XP_016878511.1:n.746+11_746+12insGGGGG
XM_024450186.1:c.818+11_818+12insGGGGG	XP_024305954.1:n.818+11_818+12insGGGGG
XM_024450187.1:c.818+11_818+12insGGGGG	XP_024305955.1:n.818+11_818+12insGGGGG
XR_001751864.2:n.1860+11_1860+12insGGGGG
XR_001751865.1:n.1807+11_1807+12insGGGGG
XR_933240.3:n.2050+11_2050+12insGGGGG
NM_001127214.4:c.1613+11_1613+12insGGGGG	NP_001120686.1:n.1613+11_1613+12insGGGGG
NM_001243279.3:c.1613+11_1613+12insGGGGG MANE Select	NP_001230208.1:n.1613+11_1613+12insGGGGG
NM_001284316.2:c.818+11_818+12insGGGGG	NP_001271245.1:n.818+11_818+12insGGGGG
NM_174917.5:c.1613+11_1613+12insGGGGG	NP_777577.2:n.1613+11_1613+12insGGGGG
NR_104293.2:n.2004+11_2004+12insGGGGG
NR_147928.2:n.2048+11_2048+12insGGGGG
NR_147929.2:n.1802+11_1802+12insGGGGG