Canonical Allele Identifier: CA2241520471

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154094G= , CM000678.2:g.89154094G=	GRCh38
NC_000016.9:g.89220502G= , CM000678.1:g.89220502G=	GRCh37
NC_000016.8:g.87748003G=	NCBI36
NG_031961.1:g.65286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1618G=	ENSP00000320646.4:p.Val540=
ENST00000614302.5:c.1618G= MANE Select	ENSP00000479130.1:p.Val540=
ENST00000649953.1:c.1828G=	ENSP00000497456.1:p.Val610=
ENST00000317447.8:c.1618G=	ENSP00000320646.4:p.Val540=
ENST00000378345.8:c.823G=	ENSP00000367596.4:p.Val275=
ENST00000393145.5:n.6528G=
ENST00000406948.7:c.1618G=	ENSP00000384627.3:p.Val540=
ENST00000537116.5:n.744G=
ENST00000537155.1:n.358G=
ENST00000542688.5:c.*362G=	ENSP00000446281.1:n.*362G=
ENST00000614302.4:c.1618G=	ENSP00000479130.1:p.Val540=
NM_001127214.3:c.1618G=	NP_001120686.1:p.Val540=
NM_001243279.2:c.1618G=	NP_001230208.1:p.Val540=
NM_001284316.1:c.823G=	NP_001271245.1:p.Val275=
NM_174917.4:c.1618G=	NP_777577.2:p.Val540=
NR_045667.2:n.744G=
NR_104293.1:n.2052G=
XR_933239.1:n.2059G=
XR_933240.1:n.2056G=
XR_933241.1:n.1813G=
NR_147928.1:n.2096G=
NR_147929.1:n.1850G=
XM_017023020.2:c.-3487G=	XP_016878509.1:n.-3487G=
XM_024450187.1:c.823G=	XP_024305955.1:p.Val275=
XR_001751864.2:n.1865G=
XR_933240.3:n.2055G=
NM_001127214.4:c.1618G=	NP_001120686.1:p.Val540=
NM_001243279.3:c.1618G= MANE Select	NP_001230208.1:p.Val540=
NM_001284316.2:c.823G=	NP_001271245.1:p.Val275=
NM_174917.5:c.1618G=	NP_777577.2:p.Val540=
NR_104293.2:n.2009G=
NR_147928.2:n.2053G=
NR_147929.2:n.1807G=