Canonical Allele Identifier: CA1979721633
Gene: ACTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560719C= , CM000673.2:g.66560719C= GRCh38
NC_000011.9:g.66328190C= , CM000673.1:g.66328190C= GRCh37
NC_000011.8:g.66084766C= NCBI36
NG_013304.2:g.18800C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1824C= MANE Select ENSP00000426797.1:p.Thr608=
ENST00000502692.5:c.1953C= ENSP00000422007.1:p.Thr651=
ENST00000513398.1:c.1824C= ENSP00000426797.1:p.Thr608=
NM_001104.3:c.1824C= NP_001095.2:p.Thr608=
NM_001258371.2:c.1953C= NP_001245300.2:p.Thr651=
NM_001104.4:c.1824C= MANE Select NP_001095.2:p.Thr608=
NM_001258371.3:c.1953C= NP_001245300.2:p.Thr651=