Canonical Allele Identifier: CA2241520474
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89154097C= , CM000678.2:g.89154097C= GRCh38
NC_000016.9:g.89220505C= , CM000678.1:g.89220505C= GRCh37
NC_000016.8:g.87748006C= NCBI36
NG_031961.1:g.65289C=

Transcript Alleles

HGVS Amino-acid change
ENST00000317447.9:c.1621C= ENSP00000320646.4:p.Leu541=
ENST00000614302.5:c.1621C= MANE Select ENSP00000479130.1:p.Leu541=
ENST00000649953.1:c.1831C= ENSP00000497456.1:p.Leu611=
ENST00000317447.8:c.1621C= ENSP00000320646.4:p.Leu541=
ENST00000378345.8:c.826C= ENSP00000367596.4:p.Leu276=
ENST00000393145.5:n.6531C=
ENST00000406948.7:c.1621C= ENSP00000384627.3:p.Leu541=
ENST00000537116.5:n.747C=
ENST00000537155.1:n.361C=
ENST00000542688.5:c.*365C= ENSP00000446281.1:n.*365C=
ENST00000614302.4:c.1621C= ENSP00000479130.1:p.Leu541=
NM_001127214.3:c.1621C= NP_001120686.1:p.Leu541=
NM_001243279.2:c.1621C= NP_001230208.1:p.Leu541=
NM_001284316.1:c.826C= NP_001271245.1:p.Leu276=
NM_174917.4:c.1621C= NP_777577.2:p.Leu541=
NR_045667.2:n.747C=
NR_104293.1:n.2055C=
XR_933239.1:n.2062C=
XR_933240.1:n.2059C=
XR_933241.1:n.1816C=
NR_147928.1:n.2099C=
NR_147929.1:n.1853C=
XM_017023020.2:c.-3484C= XP_016878509.1:n.-3484C=
XM_024450187.1:c.826C= XP_024305955.1:p.Leu276=
XR_001751864.2:n.1868C=
XR_933240.3:n.2058C=
NM_001127214.4:c.1621C= NP_001120686.1:p.Leu541=
NM_001243279.3:c.1621C= MANE Select NP_001230208.1:p.Leu541=
NM_001284316.2:c.826C= NP_001271245.1:p.Leu276=
NM_174917.5:c.1621C= NP_777577.2:p.Leu541=
NR_104293.2:n.2012C=
NR_147928.2:n.2056C=
NR_147929.2:n.1810C=