Canonical Allele Identifier: CA397149055

Gene: ACSF3

Linked Data

• dbSNP Id: rs369726475
• gnomAD v2: 16-89212412-G-C
• gnomAD v3: 16-89146004-G-C
• gnomAD v4: 16-89146004-G-C
• MyVariant Identifiers: chr16:g.89212412G>C (hg19) ; chr16:g.89146004G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146004G>C , CM000678.2:g.89146004G>C	GRCh38
NC_000016.9:g.89212412G>C , CM000678.1:g.89212412G>C	GRCh37
NC_000016.8:g.87739913G>C	NCBI36
NG_031961.1:g.57196G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1568G>C	ENSP00000320646.4:p.Arg523Pro
ENST00000614302.5:c.1568G>C MANE Select	ENSP00000479130.1:p.Arg523Pro
ENST00000649953.1:c.1778G>C	ENSP00000497456.1:p.Arg593Pro
ENST00000317447.8:c.1568G>C	ENSP00000320646.4:p.Arg523Pro
ENST00000378345.8:c.773G>C	ENSP00000367596.4:p.Arg258Pro
ENST00000406948.7:c.1568G>C	ENSP00000384627.3:p.Arg523Pro
ENST00000535176.1:c.55G>C
ENST00000537116.5:n.694G>C
ENST00000537155.1:n.308G>C
ENST00000542688.5:c.*312G>C	ENSP00000446281.1:n.*312G>C
ENST00000562204.1:n.541G>C
ENST00000614302.4:c.1568G>C	ENSP00000479130.1:p.Arg523Pro
NM_001127214.3:c.1568G>C	NP_001120686.1:p.Arg523Pro
NM_001243279.2:c.1568G>C	NP_001230208.1:p.Arg523Pro
NM_001284316.1:c.773G>C	NP_001271245.1:p.Arg258Pro
NM_174917.4:c.1568G>C	NP_777577.2:p.Arg523Pro
NR_045667.2:n.694G>C
NR_104293.1:n.2002G>C
XM_005256293.1:c.1568G>C	XP_005256350.1:p.Arg523Pro
XM_011522942.1:c.1568G>C	XP_011521244.1:p.Arg523Pro
XM_011522943.1:c.1568G>C	XP_011521245.1:p.Arg523Pro
XR_933239.1:n.2009G>C
XR_933240.1:n.2006G>C
XR_933241.1:n.1763G>C
NR_147928.1:n.2046G>C
NR_147929.1:n.1800G>C
XM_005256293.2:c.1568G>C	XP_005256350.1:p.Arg523Pro
XM_017023018.1:c.1568G>C	XP_016878507.1:p.Arg523Pro
XM_017023019.1:c.1568G>C	XP_016878508.1:p.Arg523Pro
XM_017023020.2:c.-3537G>C	XP_016878509.1:n.-3537G>C
XM_017023022.1:c.701G>C	XP_016878511.1:p.Arg234Pro
XM_024450186.1:c.773G>C	XP_024305954.1:p.Arg258Pro
XM_024450187.1:c.773G>C	XP_024305955.1:p.Arg258Pro
XR_001751864.2:n.1815G>C
XR_001751865.1:n.1762G>C
XR_933240.3:n.2005G>C
NM_001127214.4:c.1568G>C	NP_001120686.1:p.Arg523Pro
NM_001243279.3:c.1568G>C MANE Select	NP_001230208.1:p.Arg523Pro
NM_001284316.2:c.773G>C	NP_001271245.1:p.Arg258Pro
NM_174917.5:c.1568G>C	NP_777577.2:p.Arg523Pro
NR_104293.2:n.1959G>C
NR_147928.2:n.2003G>C
NR_147929.2:n.1757G>C