Canonical Allele Identifier: CA2634920820

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89146061-T-TGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146063_89146065dup , CM000678.2:g.89146063_89146065dup	GRCh38
NC_000016.9:g.89212471_89212473dup , CM000678.1:g.89212471_89212473dup	GRCh37
NC_000016.8:g.87739972_87739974dup	NCBI36
NG_031961.1:g.57255_57257dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1613+14_1613+16dup	ENSP00000320646.4:n.1613+14_1613+16dup
ENST00000614302.5:c.1613+14_1613+16dup MANE Select	ENSP00000479130.1:n.1613+14_1613+16dup
ENST00000649953.1:c.1823+14_1823+16dup	ENSP00000497456.1:n.1823+14_1823+16dup
ENST00000317447.8:c.1613+14_1613+16dup	ENSP00000320646.4:n.1613+14_1613+16dup
ENST00000378345.8:c.818+14_818+16dup	ENSP00000367596.4:n.818+14_818+16dup
ENST00000406948.7:c.1613+14_1613+16dup	ENSP00000384627.3:n.1613+14_1613+16dup
ENST00000535176.1:c.100+14_100+16dup
ENST00000537116.5:n.739+14_739+16dup
ENST00000537155.1:n.353+14_353+16dup
ENST00000542688.5:c.*357+14_*357+16dup	ENSP00000446281.1:n.*357+14_*357+16dup
ENST00000614302.4:c.1613+14_1613+16dup	ENSP00000479130.1:n.1613+14_1613+16dup
NM_001127214.3:c.1613+14_1613+16dup	NP_001120686.1:n.1613+14_1613+16dup
NM_001243279.2:c.1613+14_1613+16dup	NP_001230208.1:n.1613+14_1613+16dup
NM_001284316.1:c.818+14_818+16dup	NP_001271245.1:n.818+14_818+16dup
NM_174917.4:c.1613+14_1613+16dup	NP_777577.2:n.1613+14_1613+16dup
NR_045667.2:n.739+14_739+16dup
NR_104293.1:n.2047+14_2047+16dup
XM_005256293.1:c.1613+14_1613+16dup	XP_005256350.1:n.1613+14_1613+16dup
XM_011522942.1:c.1613+14_1613+16dup	XP_011521244.1:n.1613+14_1613+16dup
XM_011522943.1:c.1613+14_1613+16dup	XP_011521245.1:n.1613+14_1613+16dup
XR_933239.1:n.2054+14_2054+16dup
XR_933240.1:n.2051+14_2051+16dup
XR_933241.1:n.1808+14_1808+16dup
NR_147928.1:n.2091+14_2091+16dup
NR_147929.1:n.1845+14_1845+16dup
XM_005256293.2:c.1613+14_1613+16dup	XP_005256350.1:n.1613+14_1613+16dup
XM_017023018.1:c.1613+14_1613+16dup	XP_016878507.1:n.1613+14_1613+16dup
XM_017023019.1:c.1613+14_1613+16dup	XP_016878508.1:n.1613+14_1613+16dup
XM_017023020.2:c.-3492+14_-3492+16dup	XP_016878509.1:n.-3492+14_-3492+16dup
XM_017023022.1:c.746+14_746+16dup	XP_016878511.1:n.746+14_746+16dup
XM_024450186.1:c.818+14_818+16dup	XP_024305954.1:n.818+14_818+16dup
XM_024450187.1:c.818+14_818+16dup	XP_024305955.1:n.818+14_818+16dup
XR_001751864.2:n.1860+14_1860+16dup
XR_001751865.1:n.1807+14_1807+16dup
XR_933240.3:n.2050+14_2050+16dup
NM_001127214.4:c.1613+14_1613+16dup	NP_001120686.1:n.1613+14_1613+16dup
NM_001243279.3:c.1613+14_1613+16dup MANE Select	NP_001230208.1:n.1613+14_1613+16dup
NM_001284316.2:c.818+14_818+16dup	NP_001271245.1:n.818+14_818+16dup
NM_174917.5:c.1613+14_1613+16dup	NP_777577.2:n.1613+14_1613+16dup
NR_104293.2:n.2004+14_2004+16dup
NR_147928.2:n.2048+14_2048+16dup
NR_147929.2:n.1802+14_1802+16dup