Canonical Allele Identifier: CA2241520204
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89153647_89153656delinsCCCTGCCCCA , CM000678.2:g.89153647_89153656delinsCCCTGCCCCA GRCh38
NC_000016.9:g.89220055_89220064delinsCCCTGCCCCA , CM000678.1:g.89220055_89220064delinsCCCTGCCCCA GRCh37
NC_000016.8:g.87747556_87747565delinsCCCTGCCCCA NCBI36
NG_031961.1:g.64839_64848delinsCCCTGCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1614-443_1614-434delinsCCCTGCCCCA ENSP00000320646.4:n.1614-443_1614-434delinsCCCTGCCCCA
ENST00000614302.5:c.1614-443_1614-434delinsCCCTGCCCCA MANE Select ENSP00000479130.1:n.1614-443_1614-434delinsCCCTGCCCCA
ENST00000649953.1:c.1824-443_1824-434delinsCCCTGCCCCA ENSP00000497456.1:n.1824-443_1824-434delinsCCCTGCCCCA
ENST00000317447.8:c.1614-443_1614-434delinsCCCTGCCCCA ENSP00000320646.4:n.1614-443_1614-434delinsCCCTGCCCCA
ENST00000378345.8:c.819-443_819-434delinsCCCTGCCCCA ENSP00000367596.4:n.819-443_819-434delinsCCCTGCCCCA
ENST00000393145.5:n.6081_6090delinsCCCTGCCCCA
ENST00000406948.7:c.1614-443_1614-434delinsCCCTGCCCCA ENSP00000384627.3:n.1614-443_1614-434delinsCCCTGCCCCA
ENST00000537116.5:n.740-443_740-434delinsCCCTGCCCCA
ENST00000537155.1:n.354-443_354-434delinsCCCTGCCCCA
ENST00000542688.5:c.*358-443_*358-434delinsCCCTGCCCCA ENSP00000446281.1:n.*358-443_*358-434delinsCCCTGCCCCA
ENST00000614302.4:c.1614-443_1614-434delinsCCCTGCCCCA ENSP00000479130.1:n.1614-443_1614-434delinsCCCTGCCCCA
NM_001127214.3:c.1614-443_1614-434delinsCCCTGCCCCA NP_001120686.1:n.1614-443_1614-434delinsCCCTGCCCCA
NM_001243279.2:c.1614-443_1614-434delinsCCCTGCCCCA NP_001230208.1:n.1614-443_1614-434delinsCCCTGCCCCA
NM_001284316.1:c.819-443_819-434delinsCCCTGCCCCA NP_001271245.1:n.819-443_819-434delinsCCCTGCCCCA
NM_174917.4:c.1614-443_1614-434delinsCCCTGCCCCA NP_777577.2:n.1614-443_1614-434delinsCCCTGCCCCA
NR_045667.2:n.740-443_740-434delinsCCCTGCCCCA
NR_104293.1:n.2048-443_2048-434delinsCCCTGCCCCA
XR_933239.1:n.2055-443_2055-434delinsCCCTGCCCCA
XR_933240.1:n.2052-443_2052-434delinsCCCTGCCCCA
XR_933241.1:n.1809-443_1809-434delinsCCCTGCCCCA
NR_147928.1:n.2092-443_2092-434delinsCCCTGCCCCA
NR_147929.1:n.1846-443_1846-434delinsCCCTGCCCCA
XM_017023020.2:c.-3491-443_-3491-434delinsCCCTGCCCCA XP_016878509.1:n.-3491-443_-3491-434delinsCCCTGCCCCA
XM_024450187.1:c.819-443_819-434delinsCCCTGCCCCA XP_024305955.1:n.819-443_819-434delinsCCCTGCCCCA
XR_001751864.2:n.1861-443_1861-434delinsCCCTGCCCCA
XR_933240.3:n.2051-443_2051-434delinsCCCTGCCCCA
NM_001127214.4:c.1614-443_1614-434delinsCCCTGCCCCA NP_001120686.1:n.1614-443_1614-434delinsCCCTGCCCCA
NM_001243279.3:c.1614-443_1614-434delinsCCCTGCCCCA MANE Select NP_001230208.1:n.1614-443_1614-434delinsCCCTGCCCCA
NM_001284316.2:c.819-443_819-434delinsCCCTGCCCCA NP_001271245.1:n.819-443_819-434delinsCCCTGCCCCA
NM_174917.5:c.1614-443_1614-434delinsCCCTGCCCCA NP_777577.2:n.1614-443_1614-434delinsCCCTGCCCCA
NR_104293.2:n.2005-443_2005-434delinsCCCTGCCCCA
NR_147928.2:n.2049-443_2049-434delinsCCCTGCCCCA
NR_147929.2:n.1803-443_1803-434delinsCCCTGCCCCA