Canonical Allele Identifier: CA2241515799

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145983T= , CM000678.2:g.89145983T=	GRCh38
NC_000016.9:g.89212391T= , CM000678.1:g.89212391T=	GRCh37
NC_000016.8:g.87739892T=	NCBI36
NG_031961.1:g.57175T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1547T=	ENSP00000320646.4:p.Val516=
ENST00000614302.5:c.1547T= MANE Select	ENSP00000479130.1:p.Val516=
ENST00000649953.1:c.1757T=	ENSP00000497456.1:p.Val586=
ENST00000317447.8:c.1547T=	ENSP00000320646.4:p.Val516=
ENST00000378345.8:c.752T=	ENSP00000367596.4:p.Val251=
ENST00000406948.7:c.1547T=	ENSP00000384627.3:p.Val516=
ENST00000535176.1:c.34T=
ENST00000537116.5:n.673T=
ENST00000537155.1:n.287T=
ENST00000542688.5:c.*291T=	ENSP00000446281.1:n.*291T=
ENST00000562204.1:n.520T=
ENST00000614302.4:c.1547T=	ENSP00000479130.1:p.Val516=
NM_001127214.3:c.1547T=	NP_001120686.1:p.Val516=
NM_001243279.2:c.1547T=	NP_001230208.1:p.Val516=
NM_001284316.1:c.752T=	NP_001271245.1:p.Val251=
NM_174917.4:c.1547T=	NP_777577.2:p.Val516=
NR_045667.2:n.673T=
NR_104293.1:n.1981T=
XM_005256293.1:c.1547T=	XP_005256350.1:p.Val516=
XM_011522942.1:c.1547T=	XP_011521244.1:p.Val516=
XM_011522943.1:c.1547T=	XP_011521245.1:p.Val516=
XR_933239.1:n.1988T=
XR_933240.1:n.1985T=
XR_933241.1:n.1742T=
NR_147928.1:n.2025T=
NR_147929.1:n.1779T=
XM_005256293.2:c.1547T=	XP_005256350.1:p.Val516=
XM_017023018.1:c.1547T=	XP_016878507.1:p.Val516=
XM_017023019.1:c.1547T=	XP_016878508.1:p.Val516=
XM_017023020.2:c.-3558T=	XP_016878509.1:n.-3558T=
XM_017023022.1:c.680T=	XP_016878511.1:p.Val227=
XM_024450186.1:c.752T=	XP_024305954.1:p.Val251=
XM_024450187.1:c.752T=	XP_024305955.1:p.Val251=
XR_001751864.2:n.1794T=
XR_001751865.1:n.1741T=
XR_933240.3:n.1984T=
NM_001127214.4:c.1547T=	NP_001120686.1:p.Val516=
NM_001243279.3:c.1547T= MANE Select	NP_001230208.1:p.Val516=
NM_001284316.2:c.752T=	NP_001271245.1:p.Val251=
NM_174917.5:c.1547T=	NP_777577.2:p.Val516=
NR_104293.2:n.1938T=
NR_147928.2:n.1982T=
NR_147929.2:n.1736T=