Canonical Allele Identifier: CA624225311

Gene: ACSF3

Linked Data

• ClinVar Variation Id: 1321583
• ClinVar RCV Id: RCV001779675
• dbSNP Id: rs1430683913
• gnomAD v2: 16-89212469-T-G
• gnomAD v3: 16-89146061-T-G
• gnomAD v4: 16-89146061-T-G
• MyVariant Identifiers: chr16:g.89212469T>G (hg19) ; chr16:g.89212469_89212470delinsGG (hg19) ; chr16:g.89146061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146061T>G , CM000678.2:g.89146061T>G	GRCh38
NC_000016.9:g.89212469T>G , CM000678.1:g.89212469T>G	GRCh37
NC_000016.8:g.87739970T>G	NCBI36
NG_031961.1:g.57253T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1613+12T>G	ENSP00000320646.4:n.1613+12T>G
ENST00000614302.5:c.1613+12T>G MANE Select	ENSP00000479130.1:n.1613+12T>G
ENST00000649953.1:c.1823+12T>G	ENSP00000497456.1:n.1823+12T>G
ENST00000317447.8:c.1613+12T>G	ENSP00000320646.4:n.1613+12T>G
ENST00000378345.8:c.818+12T>G	ENSP00000367596.4:n.818+12T>G
ENST00000406948.7:c.1613+12T>G	ENSP00000384627.3:n.1613+12T>G
ENST00000535176.1:c.100+12T>G
ENST00000537116.5:n.739+12T>G
ENST00000537155.1:n.353+12T>G
ENST00000542688.5:c.*357+12T>G	ENSP00000446281.1:n.*357+12T>G
ENST00000614302.4:c.1613+12T>G	ENSP00000479130.1:n.1613+12T>G
NM_001127214.3:c.1613+12T>G	NP_001120686.1:n.1613+12T>G
NM_001243279.2:c.1613+12T>G	NP_001230208.1:n.1613+12T>G
NM_001284316.1:c.818+12T>G	NP_001271245.1:n.818+12T>G
NM_174917.4:c.1613+12T>G	NP_777577.2:n.1613+12T>G
NR_045667.2:n.739+12T>G
NR_104293.1:n.2047+12T>G
XM_005256293.1:c.1613+12T>G	XP_005256350.1:n.1613+12T>G
XM_011522942.1:c.1613+12T>G	XP_011521244.1:n.1613+12T>G
XM_011522943.1:c.1613+12T>G	XP_011521245.1:n.1613+12T>G
XR_933239.1:n.2054+12T>G
XR_933240.1:n.2051+12T>G
XR_933241.1:n.1808+12T>G
NR_147928.1:n.2091+12T>G
NR_147929.1:n.1845+12T>G
XM_005256293.2:c.1613+12T>G	XP_005256350.1:n.1613+12T>G
XM_017023018.1:c.1613+12T>G	XP_016878507.1:n.1613+12T>G
XM_017023019.1:c.1613+12T>G	XP_016878508.1:n.1613+12T>G
XM_017023020.2:c.-3492+12T>G	XP_016878509.1:n.-3492+12T>G
XM_017023022.1:c.746+12T>G	XP_016878511.1:n.746+12T>G
XM_024450186.1:c.818+12T>G	XP_024305954.1:n.818+12T>G
XM_024450187.1:c.818+12T>G	XP_024305955.1:n.818+12T>G
XR_001751864.2:n.1860+12T>G
XR_001751865.1:n.1807+12T>G
XR_933240.3:n.2050+12T>G
NM_001127214.4:c.1613+12T>G	NP_001120686.1:n.1613+12T>G
NM_001243279.3:c.1613+12T>G MANE Select	NP_001230208.1:n.1613+12T>G
NM_001284316.2:c.818+12T>G	NP_001271245.1:n.818+12T>G
NM_174917.5:c.1613+12T>G	NP_777577.2:n.1613+12T>G
NR_104293.2:n.2004+12T>G
NR_147928.2:n.2048+12T>G
NR_147929.2:n.1802+12T>G