Canonical Allele Identifier: CA8237496

Gene: ACSF3

Linked Data

• dbSNP Id: rs11273288
• ExAC: 16:89167075 C / CCCCAGGAGGCTCCTGGGAG
• gnomAD v3: 16-89100667-C-CCCCAGGAGGCTCCTGGGAG
• gnomAD v4: 16-89100667-C-CCCCAGGAGGCTCCTGGGAG
• MyVariant Identifiers: chr16:g.89167075_89167076insCCCAGGAGGCTCCTGGGAG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89100668_89100669insCCAGGAGGCTCCTGGGAGC , CM000678.2:g.89100668_89100669insCCAGGAGGCTCCTGGGAGC	GRCh38
NC_000016.9:g.89167076_89167077insCCAGGAGGCTCCTGGGAGC , CM000678.1:g.89167076_89167077insCCAGGAGGCTCCTGGGAGC	GRCh37
NC_000016.8:g.87694577_87694578insCCAGGAGGCTCCTGGGAGC	NCBI36
NG_031961.1:g.11860_11861insCCAGGAGGCTCCTGGGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000320646.4:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000614302.5:c.-14_-13insCCAGGAGGCTCCTGGGAGC MANE Select	ENSP00000479130.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000649953.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000497456.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000317447.8:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000320646.4:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000378345.8:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	ENSP00000367596.4:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC...
ENST00000406948.7:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000384627.3:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000537290.5:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000440734.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000537895.5:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	ENSP00000439201.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC...
ENST00000540697.5:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	ENSP00000445397.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC...
ENST00000541755.2:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000457301.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000542688.5:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000446281.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
ENST00000614302.4:c.-14_-13insCCAGGAGGCTCCTGGGAGC	ENSP00000479130.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NM_001127214.3:c.-14_-13insCCAGGAGGCTCCTGGGAGC	NP_001120686.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NM_001243279.2:c.-14_-13insCCAGGAGGCTCCTGGGAGC	NP_001230208.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NM_001284316.1:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	NP_001271245.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC
NM_174917.4:c.-14_-13insCCAGGAGGCTCCTGGGAGC	NP_777577.2:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NR_104293.1:n.368_369insCCAGGAGGCTCCTGGGAGC
XM_005256293.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_005256350.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_011522942.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_011521244.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_011522943.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_011521245.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_011522944.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_011521246.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XR_933238.1:n.331_332insCCAGGAGGCTCCTGGGAGC
XR_933239.1:n.331_332insCCAGGAGGCTCCTGGGAGC
XR_933240.1:n.331_332insCCAGGAGGCTCCTGGGAGC
XR_933241.1:n.331_332insCCAGGAGGCTCCTGGGAGC
NR_147928.1:n.368_369insCCAGGAGGCTCCTGGGAGC
NR_147929.1:n.368_369insCCAGGAGGCTCCTGGGAGC
XM_005256293.2:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_005256350.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_017023018.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_016878507.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_017023019.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_016878508.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_017023021.1:c.-14_-13insCCAGGAGGCTCCTGGGAGC	XP_016878510.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
XM_024450186.1:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	XP_024305954.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC
XM_024450187.1:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	XP_024305955.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC
XR_001751864.2:n.330_331insCCAGGAGGCTCCTGGGAGC
XR_001751865.1:n.330_331insCCAGGAGGCTCCTGGGAGC
XR_933238.2:n.330_331insCCAGGAGGCTCCTGGGAGC
XR_933240.3:n.330_331insCCAGGAGGCTCCTGGGAGC
NM_001127214.4:c.-14_-13insCCAGGAGGCTCCTGGGAGC	NP_001120686.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NM_001243279.3:c.-14_-13insCCAGGAGGCTCCTGGGAGC MANE Select	NP_001230208.1:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NM_001284316.2:c.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC	NP_001271245.1:n.-129-1936_-129-1935insCCAGGAGGCTCCTGGGAGC
NM_174917.5:c.-14_-13insCCAGGAGGCTCCTGGGAGC	NP_777577.2:n.-14_-13insCCAGGAGGCTCCTGGGAGC
NR_104293.2:n.325_326insCCAGGAGGCTCCTGGGAGC
NR_147928.2:n.325_326insCCAGGAGGCTCCTGGGAGC
NR_147929.2:n.325_326insCCAGGAGGCTCCTGGGAGC