Canonical Allele Identifier: CA2241520563

Gene: ACSF3

Linked Data

• dbSNP Id: rs1914468109

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154229dup , CM000678.2:g.89154229dup	GRCh38
NC_000016.9:g.89220637dup , CM000678.1:g.89220637dup	GRCh37
NC_000016.8:g.87748138dup	NCBI36
NG_031961.1:g.65421dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*22dup	ENSP00000320646.4:n.*22dup
ENST00000614302.5:c.*22dup MANE Select	ENSP00000479130.1:n.*22dup
ENST00000649953.1:c.*22dup	ENSP00000497456.1:n.*22dup
ENST00000317447.8:c.*22dup	ENSP00000320646.4:n.*22dup
ENST00000378345.8:c.*22dup	ENSP00000367596.4:n.*22dup
ENST00000393145.5:n.6663dup
ENST00000406948.7:c.*22dup	ENSP00000384627.3:n.*22dup
ENST00000537116.5:n.879dup
ENST00000537155.1:n.493dup
ENST00000542688.5:c.*497dup	ENSP00000446281.1:n.*497dup
ENST00000614302.4:c.*22dup	ENSP00000479130.1:n.*22dup
NM_001127214.3:c.*22dup	NP_001120686.1:n.*22dup
NM_001243279.2:c.*22dup	NP_001230208.1:n.*22dup
NM_001284316.1:c.*22dup	NP_001271245.1:n.*22dup
NM_174917.4:c.*22dup	NP_777577.2:n.*22dup
NR_045667.2:n.879dup
NR_104293.1:n.2187dup
XR_933239.1:n.2194dup
XR_933240.1:n.2191dup
XR_933241.1:n.1948dup
NR_147928.1:n.2231dup
NR_147929.1:n.1985dup
XM_017023020.2:c.-3352dup	XP_016878509.1:n.-3352dup
XM_024450187.1:c.*22dup	XP_024305955.1:n.*22dup
XR_001751864.2:n.2000dup
XR_933240.3:n.2190dup
NM_001127214.4:c.*22dup	NP_001120686.1:n.*22dup
NM_001243279.3:c.*22dup MANE Select	NP_001230208.1:n.*22dup
NM_001284316.2:c.*22dup	NP_001271245.1:n.*22dup
NM_174917.5:c.*22dup	NP_777577.2:n.*22dup
NR_104293.2:n.2144dup
NR_147928.2:n.2188dup
NR_147929.2:n.1942dup