Canonical Allele Identifier: CA2634921080

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154303-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154303A>C , CM000678.2:g.89154303A>C	GRCh38
NC_000016.9:g.89220711A>C , CM000678.1:g.89220711A>C	GRCh37
NC_000016.8:g.87748212A>C	NCBI36
NG_031961.1:g.65495A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*96A>C	ENSP00000320646.4:n.*96A>C
ENST00000614302.5:c.*96A>C MANE Select	ENSP00000479130.1:n.*96A>C
ENST00000649953.1:c.*96A>C	ENSP00000497456.1:n.*96A>C
ENST00000317447.8:c.*96A>C	ENSP00000320646.4:n.*96A>C
ENST00000378345.8:c.*96A>C	ENSP00000367596.4:n.*96A>C
ENST00000393145.5:n.6737A>C
ENST00000406948.7:c.*96A>C	ENSP00000384627.3:n.*96A>C
ENST00000537116.5:n.953A>C
ENST00000537155.1:n.567A>C
ENST00000542688.5:c.*571A>C	ENSP00000446281.1:n.*571A>C
ENST00000614302.4:c.*96A>C	ENSP00000479130.1:n.*96A>C
NM_001127214.3:c.*96A>C	NP_001120686.1:n.*96A>C
NM_001243279.2:c.*96A>C	NP_001230208.1:n.*96A>C
NM_001284316.1:c.*96A>C	NP_001271245.1:n.*96A>C
NM_174917.4:c.*96A>C	NP_777577.2:n.*96A>C
NR_045667.2:n.953A>C
NR_104293.1:n.2261A>C
XR_933239.1:n.2268A>C
XR_933240.1:n.2265A>C
XR_933241.1:n.2022A>C
NR_147928.1:n.2305A>C
NR_147929.1:n.2059A>C
XM_017023020.2:c.-3278A>C	XP_016878509.1:n.-3278A>C
XM_024450187.1:c.*96A>C	XP_024305955.1:n.*96A>C
XR_001751864.2:n.2074A>C
XR_933240.3:n.2264A>C
NM_001127214.4:c.*96A>C	NP_001120686.1:n.*96A>C
NM_001243279.3:c.*96A>C MANE Select	NP_001230208.1:n.*96A>C
NM_001284316.2:c.*96A>C	NP_001271245.1:n.*96A>C
NM_174917.5:c.*96A>C	NP_777577.2:n.*96A>C
NR_104293.2:n.2218A>C
NR_147928.2:n.2262A>C
NR_147929.2:n.2016A>C