Canonical Allele Identifier: CA2634928428

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153776-GGGCCCCTCTGCCCTGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153781_89153797del , CM000678.2:g.89153781_89153797del	GRCh38
NC_000016.9:g.89220189_89220205del , CM000678.1:g.89220189_89220205del	GRCh37
NC_000016.8:g.87747690_87747706del	NCBI36
NG_031961.1:g.64973_64989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-309_1614-293del	ENSP00000320646.4:n.1614-309_1614-293del
ENST00000614302.5:c.1614-309_1614-293del MANE Select	ENSP00000479130.1:n.1614-309_1614-293del
ENST00000649953.1:c.1824-309_1824-293del	ENSP00000497456.1:n.1824-309_1824-293del
ENST00000317447.8:c.1614-309_1614-293del	ENSP00000320646.4:n.1614-309_1614-293del
ENST00000378345.8:c.819-309_819-293del	ENSP00000367596.4:n.819-309_819-293del
ENST00000393145.5:n.6215_6231del
ENST00000406948.7:c.1614-309_1614-293del	ENSP00000384627.3:n.1614-309_1614-293del
ENST00000537116.5:n.740-309_740-293del
ENST00000537155.1:n.354-309_354-293del
ENST00000542688.5:c.*358-309_*358-293del	ENSP00000446281.1:n.*358-309_*358-293del
ENST00000614302.4:c.1614-309_1614-293del	ENSP00000479130.1:n.1614-309_1614-293del
NM_001127214.3:c.1614-309_1614-293del	NP_001120686.1:n.1614-309_1614-293del
NM_001243279.2:c.1614-309_1614-293del	NP_001230208.1:n.1614-309_1614-293del
NM_001284316.1:c.819-309_819-293del	NP_001271245.1:n.819-309_819-293del
NM_174917.4:c.1614-309_1614-293del	NP_777577.2:n.1614-309_1614-293del
NR_045667.2:n.740-309_740-293del
NR_104293.1:n.2048-309_2048-293del
XR_933239.1:n.2055-309_2055-293del
XR_933240.1:n.2052-309_2052-293del
XR_933241.1:n.1809-309_1809-293del
NR_147928.1:n.2092-309_2092-293del
NR_147929.1:n.1846-309_1846-293del
XM_017023020.2:c.-3491-309_-3491-293del	XP_016878509.1:n.-3491-309_-3491-293del
XM_024450187.1:c.819-309_819-293del	XP_024305955.1:n.819-309_819-293del
XR_001751864.2:n.1861-309_1861-293del
XR_933240.3:n.2051-309_2051-293del
NM_001127214.4:c.1614-309_1614-293del	NP_001120686.1:n.1614-309_1614-293del
NM_001243279.3:c.1614-309_1614-293del MANE Select	NP_001230208.1:n.1614-309_1614-293del
NM_001284316.2:c.819-309_819-293del	NP_001271245.1:n.819-309_819-293del
NM_174917.5:c.1614-309_1614-293del	NP_777577.2:n.1614-309_1614-293del
NR_104293.2:n.2005-309_2005-293del
NR_147928.2:n.2049-309_2049-293del
NR_147929.2:n.1803-309_1803-293del