Canonical Allele Identifier: CA2241520555

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154219_89154226delinsGGGACTGC , CM000678.2:g.89154219_89154226delinsGGGACTGC	GRCh38
NC_000016.9:g.89220627_89220634delinsGGGACTGC , CM000678.1:g.89220627_89220634delinsGGGACTGC	GRCh37
NC_000016.8:g.87748128_87748135delinsGGGACTGC	NCBI36
NG_031961.1:g.65411_65418delinsGGGACTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*12_*19delinsGGGACTGC	ENSP00000320646.4:n.*12_*19delinsGGGACTGC
ENST00000614302.5:c.*12_*19delinsGGGACTGC MANE Select	ENSP00000479130.1:n.*12_*19delinsGGGACTGC
ENST00000649953.1:c.*12_*19delinsGGGACTGC	ENSP00000497456.1:n.*12_*19delinsGGGACTGC
ENST00000317447.8:c.*12_*19delinsGGGACTGC	ENSP00000320646.4:n.*12_*19delinsGGGACTGC
ENST00000378345.8:c.*12_*19delinsGGGACTGC	ENSP00000367596.4:n.*12_*19delinsGGGACTGC
ENST00000393145.5:n.6653_6660delinsGGGACTGC
ENST00000406948.7:c.*12_*19delinsGGGACTGC	ENSP00000384627.3:n.*12_*19delinsGGGACTGC
ENST00000537116.5:n.869_876delinsGGGACTGC
ENST00000537155.1:n.483_490delinsGGGACTGC
ENST00000542688.5:c.*487_*494delinsGGGACTGC	ENSP00000446281.1:n.*487_*494delinsGGGACTGC
ENST00000614302.4:c.*12_*19delinsGGGACTGC	ENSP00000479130.1:n.*12_*19delinsGGGACTGC
NM_001127214.3:c.*12_*19delinsGGGACTGC	NP_001120686.1:n.*12_*19delinsGGGACTGC
NM_001243279.2:c.*12_*19delinsGGGACTGC	NP_001230208.1:n.*12_*19delinsGGGACTGC
NM_001284316.1:c.*12_*19delinsGGGACTGC	NP_001271245.1:n.*12_*19delinsGGGACTGC
NM_174917.4:c.*12_*19delinsGGGACTGC	NP_777577.2:n.*12_*19delinsGGGACTGC
NR_045667.2:n.869_876delinsGGGACTGC
NR_104293.1:n.2177_2184delinsGGGACTGC
XR_933239.1:n.2184_2191delinsGGGACTGC
XR_933240.1:n.2181_2188delinsGGGACTGC
XR_933241.1:n.1938_1945delinsGGGACTGC
NR_147928.1:n.2221_2228delinsGGGACTGC
NR_147929.1:n.1975_1982delinsGGGACTGC
XM_017023020.2:c.-3362_-3355delinsGGGACTGC	XP_016878509.1:n.-3362_-3355delinsGGGACTGC
XM_024450187.1:c.*12_*19delinsGGGACTGC	XP_024305955.1:n.*12_*19delinsGGGACTGC
XR_001751864.2:n.1990_1997delinsGGGACTGC
XR_933240.3:n.2180_2187delinsGGGACTGC
NM_001127214.4:c.*12_*19delinsGGGACTGC	NP_001120686.1:n.*12_*19delinsGGGACTGC
NM_001243279.3:c.*12_*19delinsGGGACTGC MANE Select	NP_001230208.1:n.*12_*19delinsGGGACTGC
NM_001284316.2:c.*12_*19delinsGGGACTGC	NP_001271245.1:n.*12_*19delinsGGGACTGC
NM_174917.5:c.*12_*19delinsGGGACTGC	NP_777577.2:n.*12_*19delinsGGGACTGC
NR_104293.2:n.2134_2141delinsGGGACTGC
NR_147928.2:n.2178_2185delinsGGGACTGC
NR_147929.2:n.1932_1939delinsGGGACTGC