Canonical Allele Identifier: CA497148510

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220595A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154187A>C , CM000678.2:g.89154187A>C	GRCh38
NC_000016.9:g.89220595A>C , CM000678.1:g.89220595A>C	GRCh37
NC_000016.8:g.87748096A>C	NCBI36
NG_031961.1:g.65379A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1711A>C	ENSP00000320646.4:p.Arg571=
ENST00000614302.5:c.1711A>C MANE Select	ENSP00000479130.1:p.Arg571=
ENST00000649953.1:c.1921A>C	ENSP00000497456.1:p.Arg641=
ENST00000317447.8:c.1711A>C	ENSP00000320646.4:p.Arg571=
ENST00000378345.8:c.916A>C	ENSP00000367596.4:p.Arg306=
ENST00000393145.5:n.6621A>C
ENST00000406948.7:c.1711A>C	ENSP00000384627.3:p.Arg571=
ENST00000537116.5:n.837A>C
ENST00000537155.1:n.451A>C
ENST00000542688.5:c.*455A>C	ENSP00000446281.1:n.*455A>C
ENST00000614302.4:c.1711A>C	ENSP00000479130.1:p.Arg571=
NM_001127214.3:c.1711A>C	NP_001120686.1:p.Arg571=
NM_001243279.2:c.1711A>C	NP_001230208.1:p.Arg571=
NM_001284316.1:c.916A>C	NP_001271245.1:p.Arg306=
NM_174917.4:c.1711A>C	NP_777577.2:p.Arg571=
NR_045667.2:n.837A>C
NR_104293.1:n.2145A>C
XR_933239.1:n.2152A>C
XR_933240.1:n.2149A>C
XR_933241.1:n.1906A>C
NR_147928.1:n.2189A>C
NR_147929.1:n.1943A>C
XM_017023020.2:c.-3394A>C	XP_016878509.1:n.-3394A>C
XM_024450187.1:c.916A>C	XP_024305955.1:p.Arg306=
XR_001751864.2:n.1958A>C
XR_933240.3:n.2148A>C
NM_001127214.4:c.1711A>C	NP_001120686.1:p.Arg571=
NM_001243279.3:c.1711A>C MANE Select	NP_001230208.1:p.Arg571=
NM_001284316.2:c.916A>C	NP_001271245.1:p.Arg306=
NM_174917.5:c.1711A>C	NP_777577.2:p.Arg571=
NR_104293.2:n.2102A>C
NR_147928.2:n.2146A>C
NR_147929.2:n.1900A>C