Canonical Allele Identifier: CA2241520490

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154115C= , CM000678.2:g.89154115C=	GRCh38
NC_000016.9:g.89220523C= , CM000678.1:g.89220523C=	GRCh37
NC_000016.8:g.87748024C=	NCBI36
NG_031961.1:g.65307C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1639C=	ENSP00000320646.4:p.Pro547=
ENST00000614302.5:c.1639C= MANE Select	ENSP00000479130.1:p.Pro547=
ENST00000649953.1:c.1849C=	ENSP00000497456.1:p.Pro617=
ENST00000317447.8:c.1639C=	ENSP00000320646.4:p.Pro547=
ENST00000378345.8:c.844C=	ENSP00000367596.4:p.Pro282=
ENST00000393145.5:n.6549C=
ENST00000406948.7:c.1639C=	ENSP00000384627.3:p.Pro547=
ENST00000537116.5:n.765C=
ENST00000537155.1:n.379C=
ENST00000542688.5:c.*383C=	ENSP00000446281.1:n.*383C=
ENST00000614302.4:c.1639C=	ENSP00000479130.1:p.Pro547=
NM_001127214.3:c.1639C=	NP_001120686.1:p.Pro547=
NM_001243279.2:c.1639C=	NP_001230208.1:p.Pro547=
NM_001284316.1:c.844C=	NP_001271245.1:p.Pro282=
NM_174917.4:c.1639C=	NP_777577.2:p.Pro547=
NR_045667.2:n.765C=
NR_104293.1:n.2073C=
XR_933239.1:n.2080C=
XR_933240.1:n.2077C=
XR_933241.1:n.1834C=
NR_147928.1:n.2117C=
NR_147929.1:n.1871C=
XM_017023020.2:c.-3466C=	XP_016878509.1:n.-3466C=
XM_024450187.1:c.844C=	XP_024305955.1:p.Pro282=
XR_001751864.2:n.1886C=
XR_933240.3:n.2076C=
NM_001127214.4:c.1639C=	NP_001120686.1:p.Pro547=
NM_001243279.3:c.1639C= MANE Select	NP_001230208.1:p.Pro547=
NM_001284316.2:c.844C=	NP_001271245.1:p.Pro282=
NM_174917.5:c.1639C=	NP_777577.2:p.Pro547=
NR_104293.2:n.2030C=
NR_147928.2:n.2074C=
NR_147929.2:n.1828C=