Canonical Allele Identifier: CA2241520542
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89154197A= , CM000678.2:g.89154197A= GRCh38
NC_000016.9:g.89220605A= , CM000678.1:g.89220605A= GRCh37
NC_000016.8:g.87748106A= NCBI36
NG_031961.1:g.65389A=

Transcript Alleles

HGVS Amino-acid change
ENST00000317447.9:c.1721A= ENSP00000320646.4:p.His574=
ENST00000614302.5:c.1721A= MANE Select ENSP00000479130.1:p.His574=
ENST00000649953.1:c.1931A= ENSP00000497456.1:p.His644=
ENST00000317447.8:c.1721A= ENSP00000320646.4:p.His574=
ENST00000378345.8:c.926A= ENSP00000367596.4:p.His309=
ENST00000393145.5:n.6631A=
ENST00000406948.7:c.1721A= ENSP00000384627.3:p.His574=
ENST00000537116.5:n.847A=
ENST00000537155.1:n.461A=
ENST00000542688.5:c.*465A= ENSP00000446281.1:n.*465A=
ENST00000614302.4:c.1721A= ENSP00000479130.1:p.His574=
NM_001127214.3:c.1721A= NP_001120686.1:p.His574=
NM_001243279.2:c.1721A= NP_001230208.1:p.His574=
NM_001284316.1:c.926A= NP_001271245.1:p.His309=
NM_174917.4:c.1721A= NP_777577.2:p.His574=
NR_045667.2:n.847A=
NR_104293.1:n.2155A=
XR_933239.1:n.2162A=
XR_933240.1:n.2159A=
XR_933241.1:n.1916A=
NR_147928.1:n.2199A=
NR_147929.1:n.1953A=
XM_017023020.2:c.-3384A= XP_016878509.1:n.-3384A=
XM_024450187.1:c.926A= XP_024305955.1:p.His309=
XR_001751864.2:n.1968A=
XR_933240.3:n.2158A=
NM_001127214.4:c.1721A= NP_001120686.1:p.His574=
NM_001243279.3:c.1721A= MANE Select NP_001230208.1:p.His574=
NM_001284316.2:c.926A= NP_001271245.1:p.His309=
NM_174917.5:c.1721A= NP_777577.2:p.His574=
NR_104293.2:n.2112A=
NR_147928.2:n.2156A=
NR_147929.2:n.1910A=