Canonical Allele Identifier: CA2634920774
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89146051_89146073del , CM000678.2:g.89146051_89146073del GRCh38
NC_000016.9:g.89212459_89212481del , CM000678.1:g.89212459_89212481del GRCh37
NC_000016.8:g.87739960_87739982del NCBI36
NG_031961.1:g.57243_57265del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1613+2_1613+24del
ENST00000614302.5:c.1613+2_1613+24del
ENST00000649953.1:c.1823+2_1823+24del
ENST00000317447.8:c.1613+2_1613+24del
ENST00000378345.8:c.818+2_818+24del
ENST00000406948.7:c.1613+2_1613+24del
ENST00000535176.1:c.100+2_100+24del
ENST00000537116.5:n.739+2_739+24del
ENST00000537155.1:n.353+2_353+24del
ENST00000542688.5:c.*357+2_*357+24del
ENST00000614302.4:c.1613+2_1613+24del
NM_001127214.3:c.1613+2_1613+24del
NM_001243279.2:c.1613+2_1613+24del
NM_001284316.1:c.818+2_818+24del
NM_174917.4:c.1613+2_1613+24del
NR_045667.2:n.739+2_739+24del
NR_104293.1:n.2047+2_2047+24del
XM_005256293.1:c.1613+2_1613+24del
XM_011522942.1:c.1613+2_1613+24del
XM_011522943.1:c.1613+2_1613+24del
XR_933239.1:n.2054+2_2054+24del
XR_933240.1:n.2051+2_2051+24del
XR_933241.1:n.1808+2_1808+24del
NR_147928.1:n.2091+2_2091+24del
NR_147929.1:n.1845+2_1845+24del
XM_005256293.2:c.1613+2_1613+24del
XM_017023018.1:c.1613+2_1613+24del
XM_017023019.1:c.1613+2_1613+24del
XM_017023020.2:c.-3492+2_-3492+24del
XM_017023022.1:c.746+2_746+24del
XM_024450186.1:c.818+2_818+24del
XM_024450187.1:c.818+2_818+24del
XR_001751864.2:n.1860+2_1860+24del
XR_001751865.1:n.1807+2_1807+24del
XR_933240.3:n.2050+2_2050+24del
NM_001127214.4:c.1613+2_1613+24del
NM_001243279.3:c.1613+2_1613+24del
NM_001284316.2:c.818+2_818+24del
NM_174917.5:c.1613+2_1613+24del
NR_104293.2:n.2004+2_2004+24del
NR_147928.2:n.2048+2_2048+24del
NR_147929.2:n.1802+2_1802+24del