Canonical Allele Identifier: CA2241520422
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89154016_89154038delinsACTGCTGGGCGCCTGAGTTCCTC , CM000678.2:g.89154016_89154038delinsACTGCTGGGCGCCTGAGTTCCTC GRCh38
NC_000016.9:g.89220424_89220446delinsACTGCTGGGCGCCTGAGTTCCTC , CM000678.1:g.89220424_89220446delinsACTGCTGGGCGCCTGAGTTCCTC GRCh37
NC_000016.8:g.87747925_87747947delinsACTGCTGGGCGCCTGAGTTCCTC NCBI36
NG_031961.1:g.65208_65230delinsACTGCTGGGCGCCTGAGTTCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000320646.4:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000614302.5:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC MANE Select ENSP00000479130.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000649953.1:c.1824-74_1824-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000497456.1:n.1824-74_1824-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000317447.8:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000320646.4:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000378345.8:c.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000367596.4:n.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCT...
ENST00000393145.5:n.6450_6472delinsACTGCTGGGCGCCTGAGTTCCTC
ENST00000406948.7:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000384627.3:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000537116.5:n.740-74_740-52delinsACTGCTGGGCGCCTGAGTTCCTC
ENST00000537155.1:n.354-74_354-52delinsACTGCTGGGCGCCTGAGTTCCTC
ENST00000542688.5:c.*358-74_*358-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000446281.1:n.*358-74_*358-52delinsACTGCTGGGCGCCTGAGTTC...
ENST00000614302.4:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC ENSP00000479130.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTC...
NM_001127214.3:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_001120686.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC...
NM_001243279.2:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_001230208.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC...
NM_001284316.1:c.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_001271245.1:n.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC
NM_174917.4:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_777577.2:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_045667.2:n.740-74_740-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_104293.1:n.2048-74_2048-52delinsACTGCTGGGCGCCTGAGTTCCTC
XR_933239.1:n.2055-74_2055-52delinsACTGCTGGGCGCCTGAGTTCCTC
XR_933240.1:n.2052-74_2052-52delinsACTGCTGGGCGCCTGAGTTCCTC
XR_933241.1:n.1809-74_1809-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_147928.1:n.2092-74_2092-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_147929.1:n.1846-74_1846-52delinsACTGCTGGGCGCCTGAGTTCCTC
XM_017023020.2:c.-3491-74_-3491-52delinsACTGCTGGGCGCCTGAGTTCCTC XP_016878509.1:n.-3491-74_-3491-52delinsACTGCTGGGCGCCTGAGTTCC...
XM_024450187.1:c.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC XP_024305955.1:n.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC
XR_001751864.2:n.1861-74_1861-52delinsACTGCTGGGCGCCTGAGTTCCTC
XR_933240.3:n.2051-74_2051-52delinsACTGCTGGGCGCCTGAGTTCCTC
NM_001127214.4:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_001120686.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC...
NM_001243279.3:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC MANE Select NP_001230208.1:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC...
NM_001284316.2:c.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_001271245.1:n.819-74_819-52delinsACTGCTGGGCGCCTGAGTTCCTC
NM_174917.5:c.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC NP_777577.2:n.1614-74_1614-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_104293.2:n.2005-74_2005-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_147928.2:n.2049-74_2049-52delinsACTGCTGGGCGCCTGAGTTCCTC
NR_147929.2:n.1803-74_1803-52delinsACTGCTGGGCGCCTGAGTTCCTC