Canonical Allele Identifier: CA2634920850
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89146069_89146070insGGGGGGTGGGGGGGGGGGGGGGGGG , CM000678.2:g.89146069_89146070insGGGGGGTGGGGGGGGGGGGGGGGGG GRCh38
NC_000016.9:g.89212477_89212478insGGGGGGTGGGGGGGGGGGGGGGGGG , CM000678.1:g.89212477_89212478insGGGGGGTGGGGGGGGGGGGGGGGGG GRCh37
NC_000016.8:g.87739978_87739979insGGGGGGTGGGGGGGGGGGGGGGGGG NCBI36
NG_031961.1:g.57261_57262insGGGGGGTGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000320646.4:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000614302.5:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG MANE Select ENSP00000479130.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000649953.1:c.1823+20_1823+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000497456.1:n.1823+20_1823+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000317447.8:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000320646.4:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000378345.8:c.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000367596.4:n.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG...
ENST00000406948.7:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000384627.3:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000535176.1:c.100+20_100+21insGGGGGGTGGGGGGGGGGGGGGGGGG
ENST00000537116.5:n.739+20_739+21insGGGGGGTGGGGGGGGGGGGGGGGGG
ENST00000537155.1:n.353+20_353+21insGGGGGGTGGGGGGGGGGGGGGGGGG
ENST00000542688.5:c.*357+20_*357+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000446281.1:n.*357+20_*357+21insGGGGGGTGGGGGGGGGGGGGGGG...
ENST00000614302.4:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG ENSP00000479130.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGG...
NM_001127214.3:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_001120686.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_001243279.2:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_001230208.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_001284316.1:c.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_001271245.1:n.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_174917.4:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_777577.2:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_045667.2:n.739+20_739+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_104293.1:n.2047+20_2047+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_005256293.1:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_005256350.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_011522942.1:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_011521244.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_011522943.1:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_011521245.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_933239.1:n.2054+20_2054+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_933240.1:n.2051+20_2051+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_933241.1:n.1808+20_1808+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_147928.1:n.2091+20_2091+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_147929.1:n.1845+20_1845+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_005256293.2:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_005256350.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_017023018.1:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_016878507.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_017023019.1:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_016878508.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_017023020.2:c.-3492+20_-3492+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_016878509.1:n.-3492+20_-3492+21insGGGGGGTGGGGGGGGGGGGGGGGG...
XM_017023022.1:c.746+20_746+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_016878511.1:n.746+20_746+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_024450186.1:c.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_024305954.1:n.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XM_024450187.1:c.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG XP_024305955.1:n.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_001751864.2:n.1860+20_1860+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_001751865.1:n.1807+20_1807+21insGGGGGGTGGGGGGGGGGGGGGGGGG
XR_933240.3:n.2050+20_2050+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_001127214.4:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_001120686.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_001243279.3:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG MANE Select NP_001230208.1:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_001284316.2:c.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_001271245.1:n.818+20_818+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NM_174917.5:c.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG NP_777577.2:n.1613+20_1613+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_104293.2:n.2004+20_2004+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_147928.2:n.2048+20_2048+21insGGGGGGTGGGGGGGGGGGGGGGGGG
NR_147929.2:n.1802+20_1802+21insGGGGGGTGGGGGGGGGGGGGGGGGG