Canonical Allele Identifier: CA2741509659
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89153893_89153894insGACGCGTGTCACGACGTCGGTATCGGTAAC , CM000678.2:g.89153893_89153894insGACGCGTGTCACGACGTCGGTATCGGTAAC GRCh38
NC_000016.9:g.89220301_89220302insGACGCGTGTCACGACGTCGGTATCGGTAAC , CM000678.1:g.89220301_89220302insGACGCGTGTCACGACGTCGGTATCGGTAAC GRCh37
NC_000016.8:g.87747802_87747803insGACGCGTGTCACGACGTCGGTATCGGTAAC NCBI36
NG_031961.1:g.65085_65086insGACGCGTGTCACGACGTCGGTATCGGTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000320646.4:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGT...
ENST00000614302.5:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC MANE Select ENSP00000479130.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGT...
ENST00000649953.1:c.1824-197_1824-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000497456.1:n.1824-197_1824-196insGACGCGTGTCACGACGTCGGT...
ENST00000317447.8:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000320646.4:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGT...
ENST00000378345.8:c.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000367596.4:n.819-197_819-196insGACGCGTGTCACGACGTCGGTAT...
ENST00000393145.5:n.6327_6328insGACGCGTGTCACGACGTCGGTATCGGTAAC
ENST00000406948.7:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000384627.3:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGT...
ENST00000537116.5:n.740-197_740-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
ENST00000537155.1:n.354-197_354-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
ENST00000542688.5:c.*358-197_*358-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000446281.1:n.*358-197_*358-196insGACGCGTGTCACGACGTCGGT...
ENST00000614302.4:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC ENSP00000479130.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGT...
NM_001127214.3:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_001120686.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATC...
NM_001243279.2:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_001230208.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATC...
NM_001284316.1:c.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_001271245.1:n.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGG...
NM_174917.4:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_777577.2:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGT...
NR_045667.2:n.740-197_740-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NR_104293.1:n.2048-197_2048-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
XR_933239.1:n.2055-197_2055-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
XR_933240.1:n.2052-197_2052-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
XR_933241.1:n.1809-197_1809-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NR_147928.1:n.2092-197_2092-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NR_147929.1:n.1846-197_1846-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
XM_017023020.2:c.-3491-197_-3491-196insGACGCGTGTCACGACGTCGGTATCGGTAAC XP_016878509.1:n.-3491-197_-3491-196insGACGCGTGTCACGACGTCGGTA...
XM_024450187.1:c.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGGTAAC XP_024305955.1:n.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGG...
XR_001751864.2:n.1861-197_1861-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
XR_933240.3:n.2051-197_2051-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NM_001127214.4:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_001120686.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATC...
NM_001243279.3:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC MANE Select NP_001230208.1:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATC...
NM_001284316.2:c.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_001271245.1:n.819-197_819-196insGACGCGTGTCACGACGTCGGTATCGG...
NM_174917.5:c.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGTAAC NP_777577.2:n.1614-197_1614-196insGACGCGTGTCACGACGTCGGTATCGGT...
NR_104293.2:n.2005-197_2005-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NR_147928.2:n.2049-197_2049-196insGACGCGTGTCACGACGTCGGTATCGGTAAC
NR_147929.2:n.1803-197_1803-196insGACGCGTGTCACGACGTCGGTATCGGTAAC