Canonical Allele Identifier: CA2241520487

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154110C= , CM000678.2:g.89154110C=	GRCh38
NC_000016.9:g.89220518C= , CM000678.1:g.89220518C=	GRCh37
NC_000016.8:g.87748019C=	NCBI36
NG_031961.1:g.65302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1634C=	ENSP00000320646.4:p.Ala545=
ENST00000614302.5:c.1634C= MANE Select	ENSP00000479130.1:p.Ala545=
ENST00000649953.1:c.1844C=	ENSP00000497456.1:p.Ala615=
ENST00000317447.8:c.1634C=	ENSP00000320646.4:p.Ala545=
ENST00000378345.8:c.839C=	ENSP00000367596.4:p.Ala280=
ENST00000393145.5:n.6544C=
ENST00000406948.7:c.1634C=	ENSP00000384627.3:p.Ala545=
ENST00000537116.5:n.760C=
ENST00000537155.1:n.374C=
ENST00000542688.5:c.*378C=	ENSP00000446281.1:n.*378C=
ENST00000614302.4:c.1634C=	ENSP00000479130.1:p.Ala545=
NM_001127214.3:c.1634C=	NP_001120686.1:p.Ala545=
NM_001243279.2:c.1634C=	NP_001230208.1:p.Ala545=
NM_001284316.1:c.839C=	NP_001271245.1:p.Ala280=
NM_174917.4:c.1634C=	NP_777577.2:p.Ala545=
NR_045667.2:n.760C=
NR_104293.1:n.2068C=
XR_933239.1:n.2075C=
XR_933240.1:n.2072C=
XR_933241.1:n.1829C=
NR_147928.1:n.2112C=
NR_147929.1:n.1866C=
XM_017023020.2:c.-3471C=	XP_016878509.1:n.-3471C=
XM_024450187.1:c.839C=	XP_024305955.1:p.Ala280=
XR_001751864.2:n.1881C=
XR_933240.3:n.2071C=
NM_001127214.4:c.1634C=	NP_001120686.1:p.Ala545=
NM_001243279.3:c.1634C= MANE Select	NP_001230208.1:p.Ala545=
NM_001284316.2:c.839C=	NP_001271245.1:p.Ala280=
NM_174917.5:c.1634C=	NP_777577.2:p.Ala545=
NR_104293.2:n.2025C=
NR_147928.2:n.2069C=
NR_147929.2:n.1823C=