Canonical Allele Identifier: CA2241515414

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145336_89145338delinsCTG , CM000678.2:g.89145336_89145338delinsCTG	GRCh38
NC_000016.9:g.89211744_89211746delinsCTG , CM000678.1:g.89211744_89211746delinsCTG	GRCh37
NC_000016.8:g.87739245_87739247delinsCTG	NCBI36
NG_031961.1:g.56528_56530delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1436_1438delinsCTG	ENSP00000320646.4:p.Thr479=
ENST00000614302.5:c.1436_1438delinsCTG MANE Select	ENSP00000479130.1:p.Thr479=
ENST00000649953.1:c.1646_1648delinsCTG	ENSP00000497456.1:p.Thr549=
ENST00000317447.8:c.1436_1438delinsCTG	ENSP00000320646.4:p.Thr479=
ENST00000378345.8:c.641_643delinsCTG	ENSP00000367596.4:p.Thr214=
ENST00000406948.7:c.1436_1438delinsCTG	ENSP00000384627.3:p.Thr479=
ENST00000537116.5:n.562_564delinsCTG
ENST00000537155.1:n.176_178delinsCTG
ENST00000542688.5:c.*180_*182delinsCTG	ENSP00000446281.1:n.*180_*182delinsCTG
ENST00000544543.5:c.641_643delinsCTG	ENSP00000442781.1:p.Thr214=
ENST00000562204.1:n.409_411delinsCTG
ENST00000614302.4:c.1436_1438delinsCTG	ENSP00000479130.1:p.Thr479=
NM_001127214.3:c.1436_1438delinsCTG	NP_001120686.1:p.Thr479=
NM_001243279.2:c.1436_1438delinsCTG	NP_001230208.1:p.Thr479=
NM_001284316.1:c.641_643delinsCTG	NP_001271245.1:p.Thr214=
NM_174917.4:c.1436_1438delinsCTG	NP_777577.2:p.Thr479=
NR_045667.2:n.562_564delinsCTG
NR_104293.1:n.1870_1872delinsCTG
XM_005256293.1:c.1436_1438delinsCTG	XP_005256350.1:p.Thr479=
XM_011522942.1:c.1436_1438delinsCTG	XP_011521244.1:p.Thr479=
XM_011522943.1:c.1436_1438delinsCTG	XP_011521245.1:p.Thr479=
XR_933239.1:n.1877_1879delinsCTG
XR_933240.1:n.1874_1876delinsCTG
XR_933241.1:n.1631_1633delinsCTG
NR_147928.1:n.1914_1916delinsCTG
NR_147929.1:n.1668_1670delinsCTG
XM_005256293.2:c.1436_1438delinsCTG	XP_005256350.1:p.Thr479=
XM_017023018.1:c.1436_1438delinsCTG	XP_016878507.1:p.Thr479=
XM_017023019.1:c.1436_1438delinsCTG	XP_016878508.1:p.Thr479=
XM_017023020.2:c.-3669_-3667delinsCTG	XP_016878509.1:n.-3669_-3667delinsCTG
XM_017023022.1:c.569_571delinsCTG	XP_016878511.1:p.Thr190=
XM_024450186.1:c.641_643delinsCTG	XP_024305954.1:p.Thr214=
XM_024450187.1:c.641_643delinsCTG	XP_024305955.1:p.Thr214=
XR_001751864.2:n.1683_1685delinsCTG
XR_001751865.1:n.1630_1632delinsCTG
XR_933240.3:n.1873_1875delinsCTG
NM_001127214.4:c.1436_1438delinsCTG	NP_001120686.1:p.Thr479=
NM_001243279.3:c.1436_1438delinsCTG MANE Select	NP_001230208.1:p.Thr479=
NM_001284316.2:c.641_643delinsCTG	NP_001271245.1:p.Thr214=
NM_174917.5:c.1436_1438delinsCTG	NP_777577.2:p.Thr479=
NR_104293.2:n.1827_1829delinsCTG
NR_147928.2:n.1871_1873delinsCTG
NR_147929.2:n.1625_1627delinsCTG