Canonical Allele Identifier: CA2241520498

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154129G= , CM000678.2:g.89154129G=	GRCh38
NC_000016.9:g.89220537G= , CM000678.1:g.89220537G=	GRCh37
NC_000016.8:g.87748038G=	NCBI36
NG_031961.1:g.65321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1653G=	ENSP00000320646.4:p.Val551=
ENST00000614302.5:c.1653G= MANE Select	ENSP00000479130.1:p.Val551=
ENST00000649953.1:c.1863G=	ENSP00000497456.1:p.Val621=
ENST00000317447.8:c.1653G=	ENSP00000320646.4:p.Val551=
ENST00000378345.8:c.858G=	ENSP00000367596.4:p.Val286=
ENST00000393145.5:n.6563G=
ENST00000406948.7:c.1653G=	ENSP00000384627.3:p.Val551=
ENST00000537116.5:n.779G=
ENST00000537155.1:n.393G=
ENST00000542688.5:c.*397G=	ENSP00000446281.1:n.*397G=
ENST00000614302.4:c.1653G=	ENSP00000479130.1:p.Val551=
NM_001127214.3:c.1653G=	NP_001120686.1:p.Val551=
NM_001243279.2:c.1653G=	NP_001230208.1:p.Val551=
NM_001284316.1:c.858G=	NP_001271245.1:p.Val286=
NM_174917.4:c.1653G=	NP_777577.2:p.Val551=
NR_045667.2:n.779G=
NR_104293.1:n.2087G=
XR_933239.1:n.2094G=
XR_933240.1:n.2091G=
XR_933241.1:n.1848G=
NR_147928.1:n.2131G=
NR_147929.1:n.1885G=
XM_017023020.2:c.-3452G=	XP_016878509.1:n.-3452G=
XM_024450187.1:c.858G=	XP_024305955.1:p.Val286=
XR_001751864.2:n.1900G=
XR_933240.3:n.2090G=
NM_001127214.4:c.1653G=	NP_001120686.1:p.Val551=
NM_001243279.3:c.1653G= MANE Select	NP_001230208.1:p.Val551=
NM_001284316.2:c.858G=	NP_001271245.1:p.Val286=
NM_174917.5:c.1653G=	NP_777577.2:p.Val551=
NR_104293.2:n.2044G=
NR_147928.2:n.2088G=
NR_147929.2:n.1842G=