Canonical Allele Identifier: CA497146217

Gene: ACSF3

Linked Data

• ClinVar Variation Id: 1110538
• ClinVar RCV Id: RCV001436813
• dbSNP Id: rs115776284
• gnomAD v3: 16-89145367-G-A
• gnomAD v4: 16-89145367-G-A
• MyVariant Identifiers: chr16:g.89211775G>A (hg19) ; chr16:g.89145367G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145367G>A , CM000678.2:g.89145367G>A	GRCh38
NC_000016.9:g.89211775G>A , CM000678.1:g.89211775G>A	GRCh37
NC_000016.8:g.87739276G>A	NCBI36
NG_031961.1:g.56559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1467G>A	ENSP00000320646.4:p.Val489=
ENST00000614302.5:c.1467G>A MANE Select	ENSP00000479130.1:p.Val489=
ENST00000649953.1:c.1677G>A	ENSP00000497456.1:p.Val559=
ENST00000317447.8:c.1467G>A	ENSP00000320646.4:p.Val489=
ENST00000378345.8:c.672G>A	ENSP00000367596.4:p.Val224=
ENST00000406948.7:c.1467G>A	ENSP00000384627.3:p.Val489=
ENST00000537116.5:n.593G>A
ENST00000537155.1:n.207G>A
ENST00000542688.5:c.*211G>A	ENSP00000446281.1:n.*211G>A
ENST00000544543.5:c.672G>A	ENSP00000442781.1:p.Val224=
ENST00000562204.1:n.440G>A
ENST00000614302.4:c.1467G>A	ENSP00000479130.1:p.Val489=
NM_001127214.3:c.1467G>A	NP_001120686.1:p.Val489=
NM_001243279.2:c.1467G>A	NP_001230208.1:p.Val489=
NM_001284316.1:c.672G>A	NP_001271245.1:p.Val224=
NM_174917.4:c.1467G>A	NP_777577.2:p.Val489=
NR_045667.2:n.593G>A
NR_104293.1:n.1901G>A
XM_005256293.1:c.1467G>A	XP_005256350.1:p.Val489=
XM_011522942.1:c.1467G>A	XP_011521244.1:p.Val489=
XM_011522943.1:c.1467G>A	XP_011521245.1:p.Val489=
XR_933239.1:n.1908G>A
XR_933240.1:n.1905G>A
XR_933241.1:n.1662G>A
NR_147928.1:n.1945G>A
NR_147929.1:n.1699G>A
XM_005256293.2:c.1467G>A	XP_005256350.1:p.Val489=
XM_017023018.1:c.1467G>A	XP_016878507.1:p.Val489=
XM_017023019.1:c.1467G>A	XP_016878508.1:p.Val489=
XM_017023020.2:c.-3638G>A	XP_016878509.1:n.-3638G>A
XM_017023022.1:c.600G>A	XP_016878511.1:p.Val200=
XM_024450186.1:c.672G>A	XP_024305954.1:p.Val224=
XM_024450187.1:c.672G>A	XP_024305955.1:p.Val224=
XR_001751864.2:n.1714G>A
XR_001751865.1:n.1661G>A
XR_933240.3:n.1904G>A
NM_001127214.4:c.1467G>A	NP_001120686.1:p.Val489=
NM_001243279.3:c.1467G>A MANE Select	NP_001230208.1:p.Val489=
NM_001284316.2:c.672G>A	NP_001271245.1:p.Val224=
NM_174917.5:c.1467G>A	NP_777577.2:p.Val489=
NR_104293.2:n.1858G>A
NR_147928.2:n.1902G>A
NR_147929.2:n.1656G>A