Canonical Allele Identifier: CA2634928010

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153620-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153622_89153623insGCA , CM000678.2:g.89153622_89153623insGCA	GRCh38
NC_000016.9:g.89220030_89220031insGCA , CM000678.1:g.89220030_89220031insGCA	GRCh37
NC_000016.8:g.87747531_87747532insGCA	NCBI36
NG_031961.1:g.64814_64815insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-468_1614-467insGCA	ENSP00000320646.4:n.1614-468_1614-467insGCA
ENST00000614302.5:c.1614-468_1614-467insGCA MANE Select	ENSP00000479130.1:n.1614-468_1614-467insGCA
ENST00000649953.1:c.1824-468_1824-467insGCA	ENSP00000497456.1:n.1824-468_1824-467insGCA
ENST00000317447.8:c.1614-468_1614-467insGCA	ENSP00000320646.4:n.1614-468_1614-467insGCA
ENST00000378345.8:c.819-468_819-467insGCA	ENSP00000367596.4:n.819-468_819-467insGCA
ENST00000393145.5:n.6056_6057insGCA
ENST00000406948.7:c.1614-468_1614-467insGCA	ENSP00000384627.3:n.1614-468_1614-467insGCA
ENST00000537116.5:n.740-468_740-467insGCA
ENST00000537155.1:n.354-468_354-467insGCA
ENST00000542688.5:c.*358-468_*358-467insGCA	ENSP00000446281.1:n.*358-468_*358-467insGCA
ENST00000614302.4:c.1614-468_1614-467insGCA	ENSP00000479130.1:n.1614-468_1614-467insGCA
NM_001127214.3:c.1614-468_1614-467insGCA	NP_001120686.1:n.1614-468_1614-467insGCA
NM_001243279.2:c.1614-468_1614-467insGCA	NP_001230208.1:n.1614-468_1614-467insGCA
NM_001284316.1:c.819-468_819-467insGCA	NP_001271245.1:n.819-468_819-467insGCA
NM_174917.4:c.1614-468_1614-467insGCA	NP_777577.2:n.1614-468_1614-467insGCA
NR_045667.2:n.740-468_740-467insGCA
NR_104293.1:n.2048-468_2048-467insGCA
XR_933239.1:n.2055-468_2055-467insGCA
XR_933240.1:n.2052-468_2052-467insGCA
XR_933241.1:n.1809-468_1809-467insGCA
NR_147928.1:n.2092-468_2092-467insGCA
NR_147929.1:n.1846-468_1846-467insGCA
XM_017023020.2:c.-3491-468_-3491-467insGCA	XP_016878509.1:n.-3491-468_-3491-467insGCA
XM_024450187.1:c.819-468_819-467insGCA	XP_024305955.1:n.819-468_819-467insGCA
XR_001751864.2:n.1861-468_1861-467insGCA
XR_933240.3:n.2051-468_2051-467insGCA
NM_001127214.4:c.1614-468_1614-467insGCA	NP_001120686.1:n.1614-468_1614-467insGCA
NM_001243279.3:c.1614-468_1614-467insGCA MANE Select	NP_001230208.1:n.1614-468_1614-467insGCA
NM_001284316.2:c.819-468_819-467insGCA	NP_001271245.1:n.819-468_819-467insGCA
NM_174917.5:c.1614-468_1614-467insGCA	NP_777577.2:n.1614-468_1614-467insGCA
NR_104293.2:n.2005-468_2005-467insGCA
NR_147928.2:n.2049-468_2049-467insGCA
NR_147929.2:n.1803-468_1803-467insGCA