Canonical Allele Identifier: CA2634921011

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154278-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154278C>T , CM000678.2:g.89154278C>T	GRCh38
NC_000016.9:g.89220686C>T , CM000678.1:g.89220686C>T	GRCh37
NC_000016.8:g.87748187C>T	NCBI36
NG_031961.1:g.65470C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*71C>T	ENSP00000320646.4:n.*71C>T
ENST00000614302.5:c.*71C>T MANE Select	ENSP00000479130.1:n.*71C>T
ENST00000649953.1:c.*71C>T	ENSP00000497456.1:n.*71C>T
ENST00000317447.8:c.*71C>T	ENSP00000320646.4:n.*71C>T
ENST00000378345.8:c.*71C>T	ENSP00000367596.4:n.*71C>T
ENST00000393145.5:n.6712C>T
ENST00000406948.7:c.*71C>T	ENSP00000384627.3:n.*71C>T
ENST00000537116.5:n.928C>T
ENST00000537155.1:n.542C>T
ENST00000542688.5:c.*546C>T	ENSP00000446281.1:n.*546C>T
ENST00000614302.4:c.*71C>T	ENSP00000479130.1:n.*71C>T
NM_001127214.3:c.*71C>T	NP_001120686.1:n.*71C>T
NM_001243279.2:c.*71C>T	NP_001230208.1:n.*71C>T
NM_001284316.1:c.*71C>T	NP_001271245.1:n.*71C>T
NM_174917.4:c.*71C>T	NP_777577.2:n.*71C>T
NR_045667.2:n.928C>T
NR_104293.1:n.2236C>T
XR_933239.1:n.2243C>T
XR_933240.1:n.2240C>T
XR_933241.1:n.1997C>T
NR_147928.1:n.2280C>T
NR_147929.1:n.2034C>T
XM_017023020.2:c.-3303C>T	XP_016878509.1:n.-3303C>T
XM_024450187.1:c.*71C>T	XP_024305955.1:n.*71C>T
XR_001751864.2:n.2049C>T
XR_933240.3:n.2239C>T
NM_001127214.4:c.*71C>T	NP_001120686.1:n.*71C>T
NM_001243279.3:c.*71C>T MANE Select	NP_001230208.1:n.*71C>T
NM_001284316.2:c.*71C>T	NP_001271245.1:n.*71C>T
NM_174917.5:c.*71C>T	NP_777577.2:n.*71C>T
NR_104293.2:n.2193C>T
NR_147928.2:n.2237C>T
NR_147929.2:n.1991C>T