Canonical Allele Identifier: CA2634928166

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153682-T-TGTTGCAGCTCAAGGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153682_89153683insGTTGCAGCTCAAGGAGA , CM000678.2:g.89153682_89153683insGTTGCAGCTCAAGGAGA	GRCh38
NC_000016.9:g.89220090_89220091insGTTGCAGCTCAAGGAGA , CM000678.1:g.89220090_89220091insGTTGCAGCTCAAGGAGA	GRCh37
NC_000016.8:g.87747591_87747592insGTTGCAGCTCAAGGAGA	NCBI36
NG_031961.1:g.64874_64875insGTTGCAGCTCAAGGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	ENSP00000320646.4:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
ENST00000614302.5:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA MANE Select	ENSP00000479130.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
ENST00000649953.1:c.1824-408_1824-407insGTTGCAGCTCAAGGAGA	ENSP00000497456.1:n.1824-408_1824-407insGTTGCAGCTCAAGGAGA
ENST00000317447.8:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	ENSP00000320646.4:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
ENST00000378345.8:c.819-408_819-407insGTTGCAGCTCAAGGAGA	ENSP00000367596.4:n.819-408_819-407insGTTGCAGCTCAAGGAGA
ENST00000393145.5:n.6116_6117insGTTGCAGCTCAAGGAGA
ENST00000406948.7:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	ENSP00000384627.3:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
ENST00000537116.5:n.740-408_740-407insGTTGCAGCTCAAGGAGA
ENST00000537155.1:n.354-408_354-407insGTTGCAGCTCAAGGAGA
ENST00000542688.5:c.*358-408_*358-407insGTTGCAGCTCAAGGAGA	ENSP00000446281.1:n.*358-408_*358-407insGTTGCAGCTCAAGGAGA
ENST00000614302.4:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	ENSP00000479130.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NM_001127214.3:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	NP_001120686.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NM_001243279.2:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	NP_001230208.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NM_001284316.1:c.819-408_819-407insGTTGCAGCTCAAGGAGA	NP_001271245.1:n.819-408_819-407insGTTGCAGCTCAAGGAGA
NM_174917.4:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	NP_777577.2:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NR_045667.2:n.740-408_740-407insGTTGCAGCTCAAGGAGA
NR_104293.1:n.2048-408_2048-407insGTTGCAGCTCAAGGAGA
XR_933239.1:n.2055-408_2055-407insGTTGCAGCTCAAGGAGA
XR_933240.1:n.2052-408_2052-407insGTTGCAGCTCAAGGAGA
XR_933241.1:n.1809-408_1809-407insGTTGCAGCTCAAGGAGA
NR_147928.1:n.2092-408_2092-407insGTTGCAGCTCAAGGAGA
NR_147929.1:n.1846-408_1846-407insGTTGCAGCTCAAGGAGA
XM_017023020.2:c.-3491-408_-3491-407insGTTGCAGCTCAAGGAGA	XP_016878509.1:n.-3491-408_-3491-407insGTTGCAGCTCAAGGAGA
XM_024450187.1:c.819-408_819-407insGTTGCAGCTCAAGGAGA	XP_024305955.1:n.819-408_819-407insGTTGCAGCTCAAGGAGA
XR_001751864.2:n.1861-408_1861-407insGTTGCAGCTCAAGGAGA
XR_933240.3:n.2051-408_2051-407insGTTGCAGCTCAAGGAGA
NM_001127214.4:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	NP_001120686.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NM_001243279.3:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA MANE Select	NP_001230208.1:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NM_001284316.2:c.819-408_819-407insGTTGCAGCTCAAGGAGA	NP_001271245.1:n.819-408_819-407insGTTGCAGCTCAAGGAGA
NM_174917.5:c.1614-408_1614-407insGTTGCAGCTCAAGGAGA	NP_777577.2:n.1614-408_1614-407insGTTGCAGCTCAAGGAGA
NR_104293.2:n.2005-408_2005-407insGTTGCAGCTCAAGGAGA
NR_147928.2:n.2049-408_2049-407insGTTGCAGCTCAAGGAGA
NR_147929.2:n.1803-408_1803-407insGTTGCAGCTCAAGGAGA