Canonical Allele Identifier: CA2241520608

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154281G= , CM000678.2:g.89154281G=	GRCh38
NC_000016.9:g.89220689G= , CM000678.1:g.89220689G=	GRCh37
NC_000016.8:g.87748190G=	NCBI36
NG_031961.1:g.65473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*74G=	ENSP00000320646.4:n.*74G=
ENST00000614302.5:c.*74G= MANE Select	ENSP00000479130.1:n.*74G=
ENST00000649953.1:c.*74G=	ENSP00000497456.1:n.*74G=
ENST00000317447.8:c.*74G=	ENSP00000320646.4:n.*74G=
ENST00000378345.8:c.*74G=	ENSP00000367596.4:n.*74G=
ENST00000393145.5:n.6715G=
ENST00000406948.7:c.*74G=	ENSP00000384627.3:n.*74G=
ENST00000537116.5:n.931G=
ENST00000537155.1:n.545G=
ENST00000542688.5:c.*549G=	ENSP00000446281.1:n.*549G=
ENST00000614302.4:c.*74G=	ENSP00000479130.1:n.*74G=
NM_001127214.3:c.*74G=	NP_001120686.1:n.*74G=
NM_001243279.2:c.*74G=	NP_001230208.1:n.*74G=
NM_001284316.1:c.*74G=	NP_001271245.1:n.*74G=
NM_174917.4:c.*74G=	NP_777577.2:n.*74G=
NR_045667.2:n.931G=
NR_104293.1:n.2239G=
XR_933239.1:n.2246G=
XR_933240.1:n.2243G=
XR_933241.1:n.2000G=
NR_147928.1:n.2283G=
NR_147929.1:n.2037G=
XM_017023020.2:c.-3300G=	XP_016878509.1:n.-3300G=
XM_024450187.1:c.*74G=	XP_024305955.1:n.*74G=
XR_001751864.2:n.2052G=
XR_933240.3:n.2242G=
NM_001127214.4:c.*74G=	NP_001120686.1:n.*74G=
NM_001243279.3:c.*74G= MANE Select	NP_001230208.1:n.*74G=
NM_001284316.2:c.*74G=	NP_001271245.1:n.*74G=
NM_174917.5:c.*74G=	NP_777577.2:n.*74G=
NR_104293.2:n.2196G=
NR_147928.2:n.2240G=
NR_147929.2:n.1994G=