Canonical Allele Identifier: CA2634920772
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89146046_89146052del , CM000678.2:g.89146046_89146052del GRCh38
NC_000016.9:g.89212454_89212460del , CM000678.1:g.89212454_89212460del GRCh37
NC_000016.8:g.87739955_87739961del NCBI36
NG_031961.1:g.57238_57244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1610_1613+3del
ENST00000614302.5:c.1610_1613+3del
ENST00000649953.1:c.1820_1823+3del
ENST00000317447.8:c.1610_1613+3del
ENST00000378345.8:c.815_818+3del
ENST00000406948.7:c.1610_1613+3del
ENST00000535176.1:c.97_100+3del
ENST00000537116.5:n.736_739+3del
ENST00000537155.1:n.350_353+3del
ENST00000542688.5:c.*354_*357+3del
ENST00000614302.4:c.1610_1613+3del
NM_001127214.3:c.1610_1613+3del
NM_001243279.2:c.1610_1613+3del
NM_001284316.1:c.815_818+3del
NM_174917.4:c.1610_1613+3del
NR_045667.2:n.736_739+3del
NR_104293.1:n.2044_2047+3del
XM_005256293.1:c.1610_1613+3del
XM_011522942.1:c.1610_1613+3del
XM_011522943.1:c.1610_1613+3del
XR_933239.1:n.2051_2054+3del
XR_933240.1:n.2048_2051+3del
XR_933241.1:n.1805_1808+3del
NR_147928.1:n.2088_2091+3del
NR_147929.1:n.1842_1845+3del
XM_005256293.2:c.1610_1613+3del
XM_017023018.1:c.1610_1613+3del
XM_017023019.1:c.1610_1613+3del
XM_017023020.2:c.-3495_-3492+3del
XM_017023022.1:c.743_746+3del
XM_024450186.1:c.815_818+3del
XM_024450187.1:c.815_818+3del
XR_001751864.2:n.1857_1860+3del
XR_001751865.1:n.1804_1807+3del
XR_933240.3:n.2047_2050+3del
NM_001127214.4:c.1610_1613+3del
NM_001243279.3:c.1610_1613+3del
NM_001284316.2:c.815_818+3del
NM_174917.5:c.1610_1613+3del
NR_104293.2:n.2001_2004+3del
NR_147928.2:n.2045_2048+3del
NR_147929.2:n.1799_1802+3del