Canonical Allele Identifier: CA1979720891
Gene: ACTN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560454G= , CM000673.2:g.66560454G= GRCh38
NC_000011.9:g.66327925G= , CM000673.1:g.66327925G= GRCh37
NC_000011.8:g.66084501G= NCBI36
NG_013304.2:g.18535G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1678-119G= MANE Select ENSP00000426797.1:n.1678-119G=
ENST00000502692.5:c.1807-119G= ENSP00000422007.1:n.1807-119G=
ENST00000513398.1:c.1678-119G= ENSP00000426797.1:n.1678-119G=
NM_001104.3:c.1678-119G= NP_001095.2:n.1678-119G=
NM_001258371.2:c.1807-119G= NP_001245300.2:n.1807-119G=
NM_001104.4:c.1678-119G= MANE Select NP_001095.2:n.1678-119G=
NM_001258371.3:c.1807-119G= NP_001245300.2:n.1807-119G=
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