Canonical Allele Identifier: CA1979721650
Gene: ACTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560728G= , CM000673.2:g.66560728G= GRCh38
NC_000011.9:g.66328199G= , CM000673.1:g.66328199G= GRCh37
NC_000011.8:g.66084775G= NCBI36
NG_013304.2:g.18809G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1833G= MANE Select ENSP00000426797.1:p.Pro611=
ENST00000502692.5:c.1962G= ENSP00000422007.1:p.Pro654=
ENST00000513398.1:c.1833G= ENSP00000426797.1:p.Pro611=
NM_001104.3:c.1833G= NP_001095.2:p.Pro611=
NM_001258371.2:c.1962G= NP_001245300.2:p.Pro654=
NM_001104.4:c.1833G= MANE Select NP_001095.2:p.Pro611=
NM_001258371.3:c.1962G= NP_001245300.2:p.Pro654=