Canonical Allele Identifier: CA2634928452

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153794-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153794_89153795insTT , CM000678.2:g.89153794_89153795insTT	GRCh38
NC_000016.9:g.89220202_89220203insTT , CM000678.1:g.89220202_89220203insTT	GRCh37
NC_000016.8:g.87747703_87747704insTT	NCBI36
NG_031961.1:g.64986_64987insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-296_1614-295insTT	ENSP00000320646.4:n.1614-296_1614-295insTT
ENST00000614302.5:c.1614-296_1614-295insTT MANE Select	ENSP00000479130.1:n.1614-296_1614-295insTT
ENST00000649953.1:c.1824-296_1824-295insTT	ENSP00000497456.1:n.1824-296_1824-295insTT
ENST00000317447.8:c.1614-296_1614-295insTT	ENSP00000320646.4:n.1614-296_1614-295insTT
ENST00000378345.8:c.819-296_819-295insTT	ENSP00000367596.4:n.819-296_819-295insTT
ENST00000393145.5:n.6228_6229insTT
ENST00000406948.7:c.1614-296_1614-295insTT	ENSP00000384627.3:n.1614-296_1614-295insTT
ENST00000537116.5:n.740-296_740-295insTT
ENST00000537155.1:n.354-296_354-295insTT
ENST00000542688.5:c.*358-296_*358-295insTT	ENSP00000446281.1:n.*358-296_*358-295insTT
ENST00000614302.4:c.1614-296_1614-295insTT	ENSP00000479130.1:n.1614-296_1614-295insTT
NM_001127214.3:c.1614-296_1614-295insTT	NP_001120686.1:n.1614-296_1614-295insTT
NM_001243279.2:c.1614-296_1614-295insTT	NP_001230208.1:n.1614-296_1614-295insTT
NM_001284316.1:c.819-296_819-295insTT	NP_001271245.1:n.819-296_819-295insTT
NM_174917.4:c.1614-296_1614-295insTT	NP_777577.2:n.1614-296_1614-295insTT
NR_045667.2:n.740-296_740-295insTT
NR_104293.1:n.2048-296_2048-295insTT
XR_933239.1:n.2055-296_2055-295insTT
XR_933240.1:n.2052-296_2052-295insTT
XR_933241.1:n.1809-296_1809-295insTT
NR_147928.1:n.2092-296_2092-295insTT
NR_147929.1:n.1846-296_1846-295insTT
XM_017023020.2:c.-3491-296_-3491-295insTT	XP_016878509.1:n.-3491-296_-3491-295insTT
XM_024450187.1:c.819-296_819-295insTT	XP_024305955.1:n.819-296_819-295insTT
XR_001751864.2:n.1861-296_1861-295insTT
XR_933240.3:n.2051-296_2051-295insTT
NM_001127214.4:c.1614-296_1614-295insTT	NP_001120686.1:n.1614-296_1614-295insTT
NM_001243279.3:c.1614-296_1614-295insTT MANE Select	NP_001230208.1:n.1614-296_1614-295insTT
NM_001284316.2:c.819-296_819-295insTT	NP_001271245.1:n.819-296_819-295insTT
NM_174917.5:c.1614-296_1614-295insTT	NP_777577.2:n.1614-296_1614-295insTT
NR_104293.2:n.2005-296_2005-295insTT
NR_147928.2:n.2049-296_2049-295insTT
NR_147929.2:n.1803-296_1803-295insTT