Canonical Allele Identifier: CA980386936

Gene: ACSF3

Linked Data

• dbSNP Id: rs1555560320
• gnomAD v3: 16-89100669-G-GGAGGCTCCCGGGAGCA
• gnomAD v4: 16-89100669-G-GGAGGCTCCCGGGAGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89100669_89100670insGAGGCTCCCGGGAGCA , CM000678.2:g.89100669_89100670insGAGGCTCCCGGGAGCA	GRCh38
NC_000016.9:g.89167077_89167078insGAGGCTCCCGGGAGCA , CM000678.1:g.89167077_89167078insGAGGCTCCCGGGAGCA	GRCh37
NC_000016.8:g.87694578_87694579insGAGGCTCCCGGGAGCA	NCBI36
NG_031961.1:g.11861_11862insGAGGCTCCCGGGAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000320646.4:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000614302.5:c.-13_-12insGAGGCTCCCGGGAGCA MANE Select	ENSP00000479130.1:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000649953.1:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000497456.1:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000317447.8:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000320646.4:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000378345.8:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	ENSP00000367596.4:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
ENST00000406948.7:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000384627.3:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000537290.5:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000440734.1:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000537895.5:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	ENSP00000439201.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
ENST00000540697.5:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	ENSP00000445397.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
ENST00000541755.2:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000457301.1:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000542688.5:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000446281.1:n.-13_-12insGAGGCTCCCGGGAGCA
ENST00000614302.4:c.-13_-12insGAGGCTCCCGGGAGCA	ENSP00000479130.1:n.-13_-12insGAGGCTCCCGGGAGCA
NM_001127214.3:c.-13_-12insGAGGCTCCCGGGAGCA	NP_001120686.1:n.-13_-12insGAGGCTCCCGGGAGCA
NM_001243279.2:c.-13_-12insGAGGCTCCCGGGAGCA	NP_001230208.1:n.-13_-12insGAGGCTCCCGGGAGCA
NM_001284316.1:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	NP_001271245.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
NM_174917.4:c.-13_-12insGAGGCTCCCGGGAGCA	NP_777577.2:n.-13_-12insGAGGCTCCCGGGAGCA
NR_104293.1:n.369_370insGAGGCTCCCGGGAGCA
XM_005256293.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_005256350.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_011522942.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_011521244.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_011522943.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_011521245.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_011522944.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_011521246.1:n.-13_-12insGAGGCTCCCGGGAGCA
XR_933238.1:n.332_333insGAGGCTCCCGGGAGCA
XR_933239.1:n.332_333insGAGGCTCCCGGGAGCA
XR_933240.1:n.332_333insGAGGCTCCCGGGAGCA
XR_933241.1:n.332_333insGAGGCTCCCGGGAGCA
NR_147928.1:n.369_370insGAGGCTCCCGGGAGCA
NR_147929.1:n.369_370insGAGGCTCCCGGGAGCA
XM_005256293.2:c.-13_-12insGAGGCTCCCGGGAGCA	XP_005256350.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_017023018.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_016878507.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_017023019.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_016878508.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_017023021.1:c.-13_-12insGAGGCTCCCGGGAGCA	XP_016878510.1:n.-13_-12insGAGGCTCCCGGGAGCA
XM_024450186.1:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	XP_024305954.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
XM_024450187.1:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	XP_024305955.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
XR_001751864.2:n.331_332insGAGGCTCCCGGGAGCA
XR_001751865.1:n.331_332insGAGGCTCCCGGGAGCA
XR_933238.2:n.331_332insGAGGCTCCCGGGAGCA
XR_933240.3:n.331_332insGAGGCTCCCGGGAGCA
NM_001127214.4:c.-13_-12insGAGGCTCCCGGGAGCA	NP_001120686.1:n.-13_-12insGAGGCTCCCGGGAGCA
NM_001243279.3:c.-13_-12insGAGGCTCCCGGGAGCA MANE Select	NP_001230208.1:n.-13_-12insGAGGCTCCCGGGAGCA
NM_001284316.2:c.-129-1935_-129-1934insGAGGCTCCCGGGAGCA	NP_001271245.1:n.-129-1935_-129-1934insGAGGCTCCCGGGAGCA
NM_174917.5:c.-13_-12insGAGGCTCCCGGGAGCA	NP_777577.2:n.-13_-12insGAGGCTCCCGGGAGCA
NR_104293.2:n.326_327insGAGGCTCCCGGGAGCA
NR_147928.2:n.326_327insGAGGCTCCCGGGAGCA
NR_147929.2:n.326_327insGAGGCTCCCGGGAGCA