Canonical Allele Identifier: CA2634920945

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154262-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154262C>T , CM000678.2:g.89154262C>T	GRCh38
NC_000016.9:g.89220670C>T , CM000678.1:g.89220670C>T	GRCh37
NC_000016.8:g.87748171C>T	NCBI36
NG_031961.1:g.65454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*55C>T	ENSP00000320646.4:n.*55C>T
ENST00000614302.5:c.*55C>T MANE Select	ENSP00000479130.1:n.*55C>T
ENST00000649953.1:c.*55C>T	ENSP00000497456.1:n.*55C>T
ENST00000317447.8:c.*55C>T	ENSP00000320646.4:n.*55C>T
ENST00000378345.8:c.*55C>T	ENSP00000367596.4:n.*55C>T
ENST00000393145.5:n.6696C>T
ENST00000406948.7:c.*55C>T	ENSP00000384627.3:n.*55C>T
ENST00000537116.5:n.912C>T
ENST00000537155.1:n.526C>T
ENST00000542688.5:c.*530C>T	ENSP00000446281.1:n.*530C>T
ENST00000614302.4:c.*55C>T	ENSP00000479130.1:n.*55C>T
NM_001127214.3:c.*55C>T	NP_001120686.1:n.*55C>T
NM_001243279.2:c.*55C>T	NP_001230208.1:n.*55C>T
NM_001284316.1:c.*55C>T	NP_001271245.1:n.*55C>T
NM_174917.4:c.*55C>T	NP_777577.2:n.*55C>T
NR_045667.2:n.912C>T
NR_104293.1:n.2220C>T
XR_933239.1:n.2227C>T
XR_933240.1:n.2224C>T
XR_933241.1:n.1981C>T
NR_147928.1:n.2264C>T
NR_147929.1:n.2018C>T
XM_017023020.2:c.-3319C>T	XP_016878509.1:n.-3319C>T
XM_024450187.1:c.*55C>T	XP_024305955.1:n.*55C>T
XR_001751864.2:n.2033C>T
XR_933240.3:n.2223C>T
NM_001127214.4:c.*55C>T	NP_001120686.1:n.*55C>T
NM_001243279.3:c.*55C>T MANE Select	NP_001230208.1:n.*55C>T
NM_001284316.2:c.*55C>T	NP_001271245.1:n.*55C>T
NM_174917.5:c.*55C>T	NP_777577.2:n.*55C>T
NR_104293.2:n.2177C>T
NR_147928.2:n.2221C>T
NR_147929.2:n.1975C>T