Canonical Allele Identifier: CA2241520517

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154159G= , CM000678.2:g.89154159G=	GRCh38
NC_000016.9:g.89220567G= , CM000678.1:g.89220567G=	GRCh37
NC_000016.8:g.87748068G=	NCBI36
NG_031961.1:g.65351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1683G=	ENSP00000320646.4:p.Met561=
ENST00000614302.5:c.1683G= MANE Select	ENSP00000479130.1:p.Met561=
ENST00000649953.1:c.1893G=	ENSP00000497456.1:p.Met631=
ENST00000317447.8:c.1683G=	ENSP00000320646.4:p.Met561=
ENST00000378345.8:c.888G=	ENSP00000367596.4:p.Met296=
ENST00000393145.5:n.6593G=
ENST00000406948.7:c.1683G=	ENSP00000384627.3:p.Met561=
ENST00000537116.5:n.809G=
ENST00000537155.1:n.423G=
ENST00000542688.5:c.*427G=	ENSP00000446281.1:n.*427G=
ENST00000614302.4:c.1683G=	ENSP00000479130.1:p.Met561=
NM_001127214.3:c.1683G=	NP_001120686.1:p.Met561=
NM_001243279.2:c.1683G=	NP_001230208.1:p.Met561=
NM_001284316.1:c.888G=	NP_001271245.1:p.Met296=
NM_174917.4:c.1683G=	NP_777577.2:p.Met561=
NR_045667.2:n.809G=
NR_104293.1:n.2117G=
XR_933239.1:n.2124G=
XR_933240.1:n.2121G=
XR_933241.1:n.1878G=
NR_147928.1:n.2161G=
NR_147929.1:n.1915G=
XM_017023020.2:c.-3422G=	XP_016878509.1:n.-3422G=
XM_024450187.1:c.888G=	XP_024305955.1:p.Met296=
XR_001751864.2:n.1930G=
XR_933240.3:n.2120G=
NM_001127214.4:c.1683G=	NP_001120686.1:p.Met561=
NM_001243279.3:c.1683G= MANE Select	NP_001230208.1:p.Met561=
NM_001284316.2:c.888G=	NP_001271245.1:p.Met296=
NM_174917.5:c.1683G=	NP_777577.2:p.Met561=
NR_104293.2:n.2074G=
NR_147928.2:n.2118G=
NR_147929.2:n.1872G=