Canonical Allele Identifier: CA2241520432

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154033_89154036delinsTTCC , CM000678.2:g.89154033_89154036delinsTTCC	GRCh38
NC_000016.9:g.89220441_89220444delinsTTCC , CM000678.1:g.89220441_89220444delinsTTCC	GRCh37
NC_000016.8:g.87747942_87747945delinsTTCC	NCBI36
NG_031961.1:g.65225_65228delinsTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-57_1614-54delinsTTCC	ENSP00000320646.4:n.1614-57_1614-54delinsTTCC
ENST00000614302.5:c.1614-57_1614-54delinsTTCC MANE Select	ENSP00000479130.1:n.1614-57_1614-54delinsTTCC
ENST00000649953.1:c.1824-57_1824-54delinsTTCC	ENSP00000497456.1:n.1824-57_1824-54delinsTTCC
ENST00000317447.8:c.1614-57_1614-54delinsTTCC	ENSP00000320646.4:n.1614-57_1614-54delinsTTCC
ENST00000378345.8:c.819-57_819-54delinsTTCC	ENSP00000367596.4:n.819-57_819-54delinsTTCC
ENST00000393145.5:n.6467_6470delinsTTCC
ENST00000406948.7:c.1614-57_1614-54delinsTTCC	ENSP00000384627.3:n.1614-57_1614-54delinsTTCC
ENST00000537116.5:n.740-57_740-54delinsTTCC
ENST00000537155.1:n.354-57_354-54delinsTTCC
ENST00000542688.5:c.*358-57_*358-54delinsTTCC	ENSP00000446281.1:n.*358-57_*358-54delinsTTCC
ENST00000614302.4:c.1614-57_1614-54delinsTTCC	ENSP00000479130.1:n.1614-57_1614-54delinsTTCC
NM_001127214.3:c.1614-57_1614-54delinsTTCC	NP_001120686.1:n.1614-57_1614-54delinsTTCC
NM_001243279.2:c.1614-57_1614-54delinsTTCC	NP_001230208.1:n.1614-57_1614-54delinsTTCC
NM_001284316.1:c.819-57_819-54delinsTTCC	NP_001271245.1:n.819-57_819-54delinsTTCC
NM_174917.4:c.1614-57_1614-54delinsTTCC	NP_777577.2:n.1614-57_1614-54delinsTTCC
NR_045667.2:n.740-57_740-54delinsTTCC
NR_104293.1:n.2048-57_2048-54delinsTTCC
XR_933239.1:n.2055-57_2055-54delinsTTCC
XR_933240.1:n.2052-57_2052-54delinsTTCC
XR_933241.1:n.1809-57_1809-54delinsTTCC
NR_147928.1:n.2092-57_2092-54delinsTTCC
NR_147929.1:n.1846-57_1846-54delinsTTCC
XM_017023020.2:c.-3491-57_-3491-54delinsTTCC	XP_016878509.1:n.-3491-57_-3491-54delinsTTCC
XM_024450187.1:c.819-57_819-54delinsTTCC	XP_024305955.1:n.819-57_819-54delinsTTCC
XR_001751864.2:n.1861-57_1861-54delinsTTCC
XR_933240.3:n.2051-57_2051-54delinsTTCC
NM_001127214.4:c.1614-57_1614-54delinsTTCC	NP_001120686.1:n.1614-57_1614-54delinsTTCC
NM_001243279.3:c.1614-57_1614-54delinsTTCC MANE Select	NP_001230208.1:n.1614-57_1614-54delinsTTCC
NM_001284316.2:c.819-57_819-54delinsTTCC	NP_001271245.1:n.819-57_819-54delinsTTCC
NM_174917.5:c.1614-57_1614-54delinsTTCC	NP_777577.2:n.1614-57_1614-54delinsTTCC
NR_104293.2:n.2005-57_2005-54delinsTTCC
NR_147928.2:n.2049-57_2049-54delinsTTCC
NR_147929.2:n.1803-57_1803-54delinsTTCC