Canonical Allele Identifier: CA2241520481

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154104_89154105delinsCG , CM000678.2:g.89154104_89154105delinsCG	GRCh38
NC_000016.9:g.89220512_89220513delinsCG , CM000678.1:g.89220512_89220513delinsCG	GRCh37
NC_000016.8:g.87748013_87748014delinsCG	NCBI36
NG_031961.1:g.65296_65297delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1628_1629delinsCG	ENSP00000320646.4:p.Pro543=
ENST00000614302.5:c.1628_1629delinsCG MANE Select	ENSP00000479130.1:p.Pro543=
ENST00000649953.1:c.1838_1839delinsCG	ENSP00000497456.1:p.Pro613=
ENST00000317447.8:c.1628_1629delinsCG	ENSP00000320646.4:p.Pro543=
ENST00000378345.8:c.833_834delinsCG	ENSP00000367596.4:p.Pro278=
ENST00000393145.5:n.6538_6539delinsCG
ENST00000406948.7:c.1628_1629delinsCG	ENSP00000384627.3:p.Pro543=
ENST00000537116.5:n.754_755delinsCG
ENST00000537155.1:n.368_369delinsCG
ENST00000542688.5:c.*372_*373delinsCG	ENSP00000446281.1:n.*372_*373delinsCG
ENST00000614302.4:c.1628_1629delinsCG	ENSP00000479130.1:p.Pro543=
NM_001127214.3:c.1628_1629delinsCG	NP_001120686.1:p.Pro543=
NM_001243279.2:c.1628_1629delinsCG	NP_001230208.1:p.Pro543=
NM_001284316.1:c.833_834delinsCG	NP_001271245.1:p.Pro278=
NM_174917.4:c.1628_1629delinsCG	NP_777577.2:p.Pro543=
NR_045667.2:n.754_755delinsCG
NR_104293.1:n.2062_2063delinsCG
XR_933239.1:n.2069_2070delinsCG
XR_933240.1:n.2066_2067delinsCG
XR_933241.1:n.1823_1824delinsCG
NR_147928.1:n.2106_2107delinsCG
NR_147929.1:n.1860_1861delinsCG
XM_017023020.2:c.-3477_-3476delinsCG	XP_016878509.1:n.-3477_-3476delinsCG
XM_024450187.1:c.833_834delinsCG	XP_024305955.1:p.Pro278=
XR_001751864.2:n.1875_1876delinsCG
XR_933240.3:n.2065_2066delinsCG
NM_001127214.4:c.1628_1629delinsCG	NP_001120686.1:p.Pro543=
NM_001243279.3:c.1628_1629delinsCG MANE Select	NP_001230208.1:p.Pro543=
NM_001284316.2:c.833_834delinsCG	NP_001271245.1:p.Pro278=
NM_174917.5:c.1628_1629delinsCG	NP_777577.2:p.Pro543=
NR_104293.2:n.2019_2020delinsCG
NR_147928.2:n.2063_2064delinsCG
NR_147929.2:n.1817_1818delinsCG