Canonical Allele Identifier: CA2241520598

Gene: ACSF3

Linked Data

• dbSNP Id: rs1914474473
• gnomAD v4: 16-89154272-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154272C>G , CM000678.2:g.89154272C>G	GRCh38
NC_000016.9:g.89220680C>G , CM000678.1:g.89220680C>G	GRCh37
NC_000016.8:g.87748181C>G	NCBI36
NG_031961.1:g.65464C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*65C>G	ENSP00000320646.4:n.*65C>G
ENST00000614302.5:c.*65C>G MANE Select	ENSP00000479130.1:n.*65C>G
ENST00000649953.1:c.*65C>G	ENSP00000497456.1:n.*65C>G
ENST00000317447.8:c.*65C>G	ENSP00000320646.4:n.*65C>G
ENST00000378345.8:c.*65C>G	ENSP00000367596.4:n.*65C>G
ENST00000393145.5:n.6706C>G
ENST00000406948.7:c.*65C>G	ENSP00000384627.3:n.*65C>G
ENST00000537116.5:n.922C>G
ENST00000537155.1:n.536C>G
ENST00000542688.5:c.*540C>G	ENSP00000446281.1:n.*540C>G
ENST00000614302.4:c.*65C>G	ENSP00000479130.1:n.*65C>G
NM_001127214.3:c.*65C>G	NP_001120686.1:n.*65C>G
NM_001243279.2:c.*65C>G	NP_001230208.1:n.*65C>G
NM_001284316.1:c.*65C>G	NP_001271245.1:n.*65C>G
NM_174917.4:c.*65C>G	NP_777577.2:n.*65C>G
NR_045667.2:n.922C>G
NR_104293.1:n.2230C>G
XR_933239.1:n.2237C>G
XR_933240.1:n.2234C>G
XR_933241.1:n.1991C>G
NR_147928.1:n.2274C>G
NR_147929.1:n.2028C>G
XM_017023020.2:c.-3309C>G	XP_016878509.1:n.-3309C>G
XM_024450187.1:c.*65C>G	XP_024305955.1:n.*65C>G
XR_001751864.2:n.2043C>G
XR_933240.3:n.2233C>G
NM_001127214.4:c.*65C>G	NP_001120686.1:n.*65C>G
NM_001243279.3:c.*65C>G MANE Select	NP_001230208.1:n.*65C>G
NM_001284316.2:c.*65C>G	NP_001271245.1:n.*65C>G
NM_174917.5:c.*65C>G	NP_777577.2:n.*65C>G
NR_104293.2:n.2187C>G
NR_147928.2:n.2231C>G
NR_147929.2:n.1985C>G