Canonical Allele Identifier: CA2241520569

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154232T= , CM000678.2:g.89154232T=	GRCh38
NC_000016.9:g.89220640T= , CM000678.1:g.89220640T=	GRCh37
NC_000016.8:g.87748141T=	NCBI36
NG_031961.1:g.65424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.*25T=	ENSP00000320646.4:n.*25T=
ENST00000614302.5:c.*25T= MANE Select	ENSP00000479130.1:n.*25T=
ENST00000649953.1:c.*25T=	ENSP00000497456.1:n.*25T=
ENST00000317447.8:c.*25T=	ENSP00000320646.4:n.*25T=
ENST00000378345.8:c.*25T=	ENSP00000367596.4:n.*25T=
ENST00000393145.5:n.6666T=
ENST00000406948.7:c.*25T=	ENSP00000384627.3:n.*25T=
ENST00000537116.5:n.882T=
ENST00000537155.1:n.496T=
ENST00000542688.5:c.*500T=	ENSP00000446281.1:n.*500T=
ENST00000614302.4:c.*25T=	ENSP00000479130.1:n.*25T=
NM_001127214.3:c.*25T=	NP_001120686.1:n.*25T=
NM_001243279.2:c.*25T=	NP_001230208.1:n.*25T=
NM_001284316.1:c.*25T=	NP_001271245.1:n.*25T=
NM_174917.4:c.*25T=	NP_777577.2:n.*25T=
NR_045667.2:n.882T=
NR_104293.1:n.2190T=
XR_933239.1:n.2197T=
XR_933240.1:n.2194T=
XR_933241.1:n.1951T=
NR_147928.1:n.2234T=
NR_147929.1:n.1988T=
XM_017023020.2:c.-3349T=	XP_016878509.1:n.-3349T=
XM_024450187.1:c.*25T=	XP_024305955.1:n.*25T=
XR_001751864.2:n.2003T=
XR_933240.3:n.2193T=
NM_001127214.4:c.*25T=	NP_001120686.1:n.*25T=
NM_001243279.3:c.*25T= MANE Select	NP_001230208.1:n.*25T=
NM_001284316.2:c.*25T=	NP_001271245.1:n.*25T=
NM_174917.5:c.*25T=	NP_777577.2:n.*25T=
NR_104293.2:n.2147T=
NR_147928.2:n.2191T=
NR_147929.2:n.1945T=