Canonical Allele Identifier: CA1979720869
Gene: ACTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560436G= , CM000673.2:g.66560436G= GRCh38
NC_000011.9:g.66327907G= , CM000673.1:g.66327907G= GRCh37
NC_000011.8:g.66084483G= NCBI36
NG_013304.2:g.18517G=

Transcript Alleles

HGVS Amino-acid change
ENST00000513398.2:c.1677+125G= MANE Select ENSP00000426797.1:n.1677+125G=
ENST00000502692.5:c.1806+125G= ENSP00000422007.1:n.1806+125G=
ENST00000513398.1:c.1677+125G= ENSP00000426797.1:n.1677+125G=
NM_001104.3:c.1677+125G= NP_001095.2:n.1677+125G=
NM_001258371.2:c.1806+125G= NP_001245300.2:n.1806+125G=
NM_001104.4:c.1677+125G= MANE Select NP_001095.2:n.1677+125G=
NM_001258371.3:c.1806+125G= NP_001245300.2:n.1806+125G=