Canonical Allele Identifier: CA2169207495
Gene: ACTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34792105G= , CM000677.2:g.34792105G= GRCh38
NC_000015.9:g.35084306G= , CM000677.1:g.35084306G= GRCh37
NC_000015.8:g.32871598G= NCBI36
NG_007553.1:g.8622C= , LRG_388:g.8622C=

Transcript Alleles

HGVS Amino-acid change
ENST00000290378.6:c.793C= MANE Select ENSP00000290378.4:p.Gln265=
ENST00000647798.1:n.887C=
ENST00000650163.1:n.873C=
ENST00000290378.4:c.793C= ENSP00000290378.4:p.Gln265=
ENST00000557860.1:n.483C=
ENST00000560563.1:n.292C=
NM_005159.4:c.793C= , LRG_388t1:c.793C= NP_005150.1:p.Gln265=
NR_120329.1:n.299+14674G=
NM_005159.5:c.793C= MANE Select NP_005150.1:p.Gln265=