Canonical Allele Identifier: CA2241515382

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145274C= , CM000678.2:g.89145274C=	GRCh38
NC_000016.9:g.89211682C= , CM000678.1:g.89211682C=	GRCh37
NC_000016.8:g.87739183C=	NCBI36
NG_031961.1:g.56466C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1374C=	ENSP00000320646.4:p.Thr458=
ENST00000614302.5:c.1374C= MANE Select	ENSP00000479130.1:p.Thr458=
ENST00000649953.1:c.1584C=	ENSP00000497456.1:p.Thr528=
ENST00000317447.8:c.1374C=	ENSP00000320646.4:p.Thr458=
ENST00000378345.8:c.579C=	ENSP00000367596.4:p.Thr193=
ENST00000406948.7:c.1374C=	ENSP00000384627.3:p.Thr458=
ENST00000537116.5:n.500C=
ENST00000537155.1:n.114C=
ENST00000542688.5:c.*118C=	ENSP00000446281.1:n.*118C=
ENST00000544543.5:c.579C=	ENSP00000442781.1:p.Thr193=
ENST00000562204.1:n.347C=
ENST00000614302.4:c.1374C=	ENSP00000479130.1:p.Thr458=
NM_001127214.3:c.1374C=	NP_001120686.1:p.Thr458=
NM_001243279.2:c.1374C=	NP_001230208.1:p.Thr458=
NM_001284316.1:c.579C=	NP_001271245.1:p.Thr193=
NM_174917.4:c.1374C=	NP_777577.2:p.Thr458=
NR_045667.2:n.500C=
NR_104293.1:n.1808C=
XM_005256293.1:c.1374C=	XP_005256350.1:p.Thr458=
XM_011522942.1:c.1374C=	XP_011521244.1:p.Thr458=
XM_011522943.1:c.1374C=	XP_011521245.1:p.Thr458=
XR_933239.1:n.1815C=
XR_933240.1:n.1812C=
XR_933241.1:n.1569C=
NR_147928.1:n.1852C=
NR_147929.1:n.1606C=
XM_005256293.2:c.1374C=	XP_005256350.1:p.Thr458=
XM_017023018.1:c.1374C=	XP_016878507.1:p.Thr458=
XM_017023019.1:c.1374C=	XP_016878508.1:p.Thr458=
XM_017023020.2:c.-3731C=	XP_016878509.1:n.-3731C=
XM_017023022.1:c.507C=	XP_016878511.1:p.Thr169=
XM_024450186.1:c.579C=	XP_024305954.1:p.Thr193=
XM_024450187.1:c.579C=	XP_024305955.1:p.Thr193=
XR_001751864.2:n.1621C=
XR_001751865.1:n.1568C=
XR_933240.3:n.1811C=
NM_001127214.4:c.1374C=	NP_001120686.1:p.Thr458=
NM_001243279.3:c.1374C= MANE Select	NP_001230208.1:p.Thr458=
NM_001284316.2:c.579C=	NP_001271245.1:p.Thr193=
NM_174917.5:c.1374C=	NP_777577.2:p.Thr458=
NR_104293.2:n.1765C=
NR_147928.2:n.1809C=
NR_147929.2:n.1563C=