Canonical Allele Identifier: CA2241520528

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154175A= , CM000678.2:g.89154175A=	GRCh38
NC_000016.9:g.89220583A= , CM000678.1:g.89220583A=	GRCh37
NC_000016.8:g.87748084A=	NCBI36
NG_031961.1:g.65367A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1699A=	ENSP00000320646.4:p.Lys567=
ENST00000614302.5:c.1699A= MANE Select	ENSP00000479130.1:p.Lys567=
ENST00000649953.1:c.1909A=	ENSP00000497456.1:p.Lys637=
ENST00000317447.8:c.1699A=	ENSP00000320646.4:p.Lys567=
ENST00000378345.8:c.904A=	ENSP00000367596.4:p.Lys302=
ENST00000393145.5:n.6609A=
ENST00000406948.7:c.1699A=	ENSP00000384627.3:p.Lys567=
ENST00000537116.5:n.825A=
ENST00000537155.1:n.439A=
ENST00000542688.5:c.*443A=	ENSP00000446281.1:n.*443A=
ENST00000614302.4:c.1699A=	ENSP00000479130.1:p.Lys567=
NM_001127214.3:c.1699A=	NP_001120686.1:p.Lys567=
NM_001243279.2:c.1699A=	NP_001230208.1:p.Lys567=
NM_001284316.1:c.904A=	NP_001271245.1:p.Lys302=
NM_174917.4:c.1699A=	NP_777577.2:p.Lys567=
NR_045667.2:n.825A=
NR_104293.1:n.2133A=
XR_933239.1:n.2140A=
XR_933240.1:n.2137A=
XR_933241.1:n.1894A=
NR_147928.1:n.2177A=
NR_147929.1:n.1931A=
XM_017023020.2:c.-3406A=	XP_016878509.1:n.-3406A=
XM_024450187.1:c.904A=	XP_024305955.1:p.Lys302=
XR_001751864.2:n.1946A=
XR_933240.3:n.2136A=
NM_001127214.4:c.1699A=	NP_001120686.1:p.Lys567=
NM_001243279.3:c.1699A= MANE Select	NP_001230208.1:p.Lys567=
NM_001284316.2:c.904A=	NP_001271245.1:p.Lys302=
NM_174917.5:c.1699A=	NP_777577.2:p.Lys567=
NR_104293.2:n.2090A=
NR_147928.2:n.2134A=
NR_147929.2:n.1888A=