Canonical Allele Identifier: CA2634921086

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154311-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154311C>A , CM000678.2:g.89154311C>A	GRCh38
NC_000016.9:g.89220719C>A , CM000678.1:g.89220719C>A	GRCh37
NC_000016.8:g.87748220C>A	NCBI36
NG_031961.1:g.65503C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*104C>A	ENSP00000320646.4:n.*104C>A
ENST00000614302.5:c.*104C>A MANE Select	ENSP00000479130.1:n.*104C>A
ENST00000649953.1:c.*104C>A	ENSP00000497456.1:n.*104C>A
ENST00000317447.8:c.*104C>A	ENSP00000320646.4:n.*104C>A
ENST00000378345.8:c.*104C>A	ENSP00000367596.4:n.*104C>A
ENST00000393145.5:n.6745C>A
ENST00000406948.7:c.*104C>A	ENSP00000384627.3:n.*104C>A
ENST00000537116.5:n.961C>A
ENST00000537155.1:n.575C>A
ENST00000542688.5:c.*579C>A	ENSP00000446281.1:n.*579C>A
ENST00000614302.4:c.*104C>A	ENSP00000479130.1:n.*104C>A
NM_001127214.3:c.*104C>A	NP_001120686.1:n.*104C>A
NM_001243279.2:c.*104C>A	NP_001230208.1:n.*104C>A
NM_001284316.1:c.*104C>A	NP_001271245.1:n.*104C>A
NM_174917.4:c.*104C>A	NP_777577.2:n.*104C>A
NR_045667.2:n.961C>A
NR_104293.1:n.2269C>A
XR_933239.1:n.2276C>A
XR_933240.1:n.2273C>A
XR_933241.1:n.2030C>A
NR_147928.1:n.2313C>A
NR_147929.1:n.2067C>A
XM_017023020.2:c.-3270C>A	XP_016878509.1:n.-3270C>A
XM_024450187.1:c.*104C>A	XP_024305955.1:n.*104C>A
XR_001751864.2:n.2082C>A
XR_933240.3:n.2272C>A
NM_001127214.4:c.*104C>A	NP_001120686.1:n.*104C>A
NM_001243279.3:c.*104C>A MANE Select	NP_001230208.1:n.*104C>A
NM_001284316.2:c.*104C>A	NP_001271245.1:n.*104C>A
NM_174917.5:c.*104C>A	NP_777577.2:n.*104C>A
NR_104293.2:n.2226C>A
NR_147928.2:n.2270C>A
NR_147929.2:n.2024C>A