Canonical Allele Identifier: CA2634920768

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89146042-TGGGCCAGGTAGGGCTGGGTGGGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146047_89146070del , CM000678.2:g.89146047_89146070del	GRCh38
NC_000016.9:g.89212455_89212478del , CM000678.1:g.89212455_89212478del	GRCh37
NC_000016.8:g.87739956_87739979del	NCBI36
NG_031961.1:g.57239_57262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1611_1613+21del
ENST00000614302.5:c.1611_1613+21del
ENST00000649953.1:c.1821_1823+21del
ENST00000317447.8:c.1611_1613+21del
ENST00000378345.8:c.816_818+21del
ENST00000406948.7:c.1611_1613+21del
ENST00000535176.1:c.98_100+21del
ENST00000537116.5:n.737_739+21del
ENST00000537155.1:n.351_353+21del
ENST00000542688.5:c.*355_*357+21del
ENST00000614302.4:c.1611_1613+21del
NM_001127214.3:c.1611_1613+21del
NM_001243279.2:c.1611_1613+21del
NM_001284316.1:c.816_818+21del
NM_174917.4:c.1611_1613+21del
NR_045667.2:n.737_739+21del
NR_104293.1:n.2045_2047+21del
XM_005256293.1:c.1611_1613+21del
XM_011522942.1:c.1611_1613+21del
XM_011522943.1:c.1611_1613+21del
XR_933239.1:n.2052_2054+21del
XR_933240.1:n.2049_2051+21del
XR_933241.1:n.1806_1808+21del
NR_147928.1:n.2089_2091+21del
NR_147929.1:n.1843_1845+21del
XM_005256293.2:c.1611_1613+21del
XM_017023018.1:c.1611_1613+21del
XM_017023019.1:c.1611_1613+21del
XM_017023020.2:c.-3494_-3492+21del
XM_017023022.1:c.744_746+21del
XM_024450186.1:c.816_818+21del
XM_024450187.1:c.816_818+21del
XR_001751864.2:n.1858_1860+21del
XR_001751865.1:n.1805_1807+21del
XR_933240.3:n.2048_2050+21del
NM_001127214.4:c.1611_1613+21del
NM_001243279.3:c.1611_1613+21del
NM_001284316.2:c.816_818+21del
NM_174917.5:c.1611_1613+21del
NR_104293.2:n.2002_2004+21del
NR_147928.2:n.2046_2048+21del
NR_147929.2:n.1800_1802+21del