Canonical Allele Identifier: CA397149180

Gene: ACSF3

Linked Data

• dbSNP Id: rs1912883419
• gnomAD v4: 16-89146032-G-C
• MyVariant Identifiers: chr16:g.89212440G>C (hg19) ; chr16:g.89146032G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146032G>C , CM000678.2:g.89146032G>C	GRCh38
NC_000016.9:g.89212440G>C , CM000678.1:g.89212440G>C	GRCh37
NC_000016.8:g.87739941G>C	NCBI36
NG_031961.1:g.57224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1596G>C	ENSP00000320646.4:p.Glu532Asp
ENST00000614302.5:c.1596G>C MANE Select	ENSP00000479130.1:p.Glu532Asp
ENST00000649953.1:c.1806G>C	ENSP00000497456.1:p.Glu602Asp
ENST00000317447.8:c.1596G>C	ENSP00000320646.4:p.Glu532Asp
ENST00000378345.8:c.801G>C	ENSP00000367596.4:p.Glu267Asp
ENST00000406948.7:c.1596G>C	ENSP00000384627.3:p.Glu532Asp
ENST00000535176.1:c.83G>C
ENST00000537116.5:n.722G>C
ENST00000537155.1:n.336G>C
ENST00000542688.5:c.*340G>C	ENSP00000446281.1:n.*340G>C
ENST00000562204.1:n.569G>C
ENST00000614302.4:c.1596G>C	ENSP00000479130.1:p.Glu532Asp
NM_001127214.3:c.1596G>C	NP_001120686.1:p.Glu532Asp
NM_001243279.2:c.1596G>C	NP_001230208.1:p.Glu532Asp
NM_001284316.1:c.801G>C	NP_001271245.1:p.Glu267Asp
NM_174917.4:c.1596G>C	NP_777577.2:p.Glu532Asp
NR_045667.2:n.722G>C
NR_104293.1:n.2030G>C
XM_005256293.1:c.1596G>C	XP_005256350.1:p.Glu532Asp
XM_011522942.1:c.1596G>C	XP_011521244.1:p.Glu532Asp
XM_011522943.1:c.1596G>C	XP_011521245.1:p.Glu532Asp
XR_933239.1:n.2037G>C
XR_933240.1:n.2034G>C
XR_933241.1:n.1791G>C
NR_147928.1:n.2074G>C
NR_147929.1:n.1828G>C
XM_005256293.2:c.1596G>C	XP_005256350.1:p.Glu532Asp
XM_017023018.1:c.1596G>C	XP_016878507.1:p.Glu532Asp
XM_017023019.1:c.1596G>C	XP_016878508.1:p.Glu532Asp
XM_017023020.2:c.-3509G>C	XP_016878509.1:n.-3509G>C
XM_017023022.1:c.729G>C	XP_016878511.1:p.Glu243Asp
XM_024450186.1:c.801G>C	XP_024305954.1:p.Glu267Asp
XM_024450187.1:c.801G>C	XP_024305955.1:p.Glu267Asp
XR_001751864.2:n.1843G>C
XR_001751865.1:n.1790G>C
XR_933240.3:n.2033G>C
NM_001127214.4:c.1596G>C	NP_001120686.1:p.Glu532Asp
NM_001243279.3:c.1596G>C MANE Select	NP_001230208.1:p.Glu532Asp
NM_001284316.2:c.801G>C	NP_001271245.1:p.Glu267Asp
NM_174917.5:c.1596G>C	NP_777577.2:p.Glu532Asp
NR_104293.2:n.1987G>C
NR_147928.2:n.2031G>C
NR_147929.2:n.1785G>C