Canonical Allele Identifier: CA2241515829

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146042_89146043delinsTG , CM000678.2:g.89146042_89146043delinsTG	GRCh38
NC_000016.9:g.89212450_89212451delinsTG , CM000678.1:g.89212450_89212451delinsTG	GRCh37
NC_000016.8:g.87739951_87739952delinsTG	NCBI36
NG_031961.1:g.57234_57235delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1606_1607delinsTG	ENSP00000320646.4:p.Trp536=
ENST00000614302.5:c.1606_1607delinsTG MANE Select	ENSP00000479130.1:p.Trp536=
ENST00000649953.1:c.1816_1817delinsTG	ENSP00000497456.1:p.Trp606=
ENST00000317447.8:c.1606_1607delinsTG	ENSP00000320646.4:p.Trp536=
ENST00000378345.8:c.811_812delinsTG	ENSP00000367596.4:p.Trp271=
ENST00000406948.7:c.1606_1607delinsTG	ENSP00000384627.3:p.Trp536=
ENST00000535176.1:c.93_94delinsTG
ENST00000537116.5:n.732_733delinsTG
ENST00000537155.1:n.346_347delinsTG
ENST00000542688.5:c.*350_*351delinsTG	ENSP00000446281.1:n.*350_*351delinsTG
ENST00000562204.1:n.579_580delinsTG
ENST00000614302.4:c.1606_1607delinsTG	ENSP00000479130.1:p.Trp536=
NM_001127214.3:c.1606_1607delinsTG	NP_001120686.1:p.Trp536=
NM_001243279.2:c.1606_1607delinsTG	NP_001230208.1:p.Trp536=
NM_001284316.1:c.811_812delinsTG	NP_001271245.1:p.Trp271=
NM_174917.4:c.1606_1607delinsTG	NP_777577.2:p.Trp536=
NR_045667.2:n.732_733delinsTG
NR_104293.1:n.2040_2041delinsTG
XM_005256293.1:c.1606_1607delinsTG	XP_005256350.1:p.Trp536=
XM_011522942.1:c.1606_1607delinsTG	XP_011521244.1:p.Trp536=
XM_011522943.1:c.1606_1607delinsTG	XP_011521245.1:p.Trp536=
XR_933239.1:n.2047_2048delinsTG
XR_933240.1:n.2044_2045delinsTG
XR_933241.1:n.1801_1802delinsTG
NR_147928.1:n.2084_2085delinsTG
NR_147929.1:n.1838_1839delinsTG
XM_005256293.2:c.1606_1607delinsTG	XP_005256350.1:p.Trp536=
XM_017023018.1:c.1606_1607delinsTG	XP_016878507.1:p.Trp536=
XM_017023019.1:c.1606_1607delinsTG	XP_016878508.1:p.Trp536=
XM_017023020.2:c.-3499_-3498delinsTG	XP_016878509.1:n.-3499_-3498delinsTG
XM_017023022.1:c.739_740delinsTG	XP_016878511.1:p.Trp247=
XM_024450186.1:c.811_812delinsTG	XP_024305954.1:p.Trp271=
XM_024450187.1:c.811_812delinsTG	XP_024305955.1:p.Trp271=
XR_001751864.2:n.1853_1854delinsTG
XR_001751865.1:n.1800_1801delinsTG
XR_933240.3:n.2043_2044delinsTG
NM_001127214.4:c.1606_1607delinsTG	NP_001120686.1:p.Trp536=
NM_001243279.3:c.1606_1607delinsTG MANE Select	NP_001230208.1:p.Trp536=
NM_001284316.2:c.811_812delinsTG	NP_001271245.1:p.Trp271=
NM_174917.5:c.1606_1607delinsTG	NP_777577.2:p.Trp536=
NR_104293.2:n.1997_1998delinsTG
NR_147928.2:n.2041_2042delinsTG
NR_147929.2:n.1795_1796delinsTG