Canonical Allele Identifier: CA397150551

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154139-G-C
• MyVariant Identifiers: chr16:g.89220547G>C (hg19) ; chr16:g.89154139G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154139G>C , CM000678.2:g.89154139G>C	GRCh38
NC_000016.9:g.89220547G>C , CM000678.1:g.89220547G>C	GRCh37
NC_000016.8:g.87748048G>C	NCBI36
NG_031961.1:g.65331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1663G>C	ENSP00000320646.4:p.Glu555Gln
ENST00000614302.5:c.1663G>C MANE Select	ENSP00000479130.1:p.Glu555Gln
ENST00000649953.1:c.1873G>C	ENSP00000497456.1:p.Glu625Gln
ENST00000317447.8:c.1663G>C	ENSP00000320646.4:p.Glu555Gln
ENST00000378345.8:c.868G>C	ENSP00000367596.4:p.Glu290Gln
ENST00000393145.5:n.6573G>C
ENST00000406948.7:c.1663G>C	ENSP00000384627.3:p.Glu555Gln
ENST00000537116.5:n.789G>C
ENST00000537155.1:n.403G>C
ENST00000542688.5:c.*407G>C	ENSP00000446281.1:n.*407G>C
ENST00000614302.4:c.1663G>C	ENSP00000479130.1:p.Glu555Gln
NM_001127214.3:c.1663G>C	NP_001120686.1:p.Glu555Gln
NM_001243279.2:c.1663G>C	NP_001230208.1:p.Glu555Gln
NM_001284316.1:c.868G>C	NP_001271245.1:p.Glu290Gln
NM_174917.4:c.1663G>C	NP_777577.2:p.Glu555Gln
NR_045667.2:n.789G>C
NR_104293.1:n.2097G>C
XR_933239.1:n.2104G>C
XR_933240.1:n.2101G>C
XR_933241.1:n.1858G>C
NR_147928.1:n.2141G>C
NR_147929.1:n.1895G>C
XM_017023020.2:c.-3442G>C	XP_016878509.1:n.-3442G>C
XM_024450187.1:c.868G>C	XP_024305955.1:p.Glu290Gln
XR_001751864.2:n.1910G>C
XR_933240.3:n.2100G>C
NM_001127214.4:c.1663G>C	NP_001120686.1:p.Glu555Gln
NM_001243279.3:c.1663G>C MANE Select	NP_001230208.1:p.Glu555Gln
NM_001284316.2:c.868G>C	NP_001271245.1:p.Glu290Gln
NM_174917.5:c.1663G>C	NP_777577.2:p.Glu555Gln
NR_104293.2:n.2054G>C
NR_147928.2:n.2098G>C
NR_147929.2:n.1852G>C