Canonical Allele Identifier: CA381448072
Gene: ACTN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560741A>T , CM000673.2:g.66560741A>T GRCh38
NC_000011.9:g.66328212A>T , CM000673.1:g.66328212A>T GRCh37
NC_000011.8:g.66084788A>T NCBI36
NG_013304.2:g.18822A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1846A>T MANE Select ENSP00000426797.1:p.Thr616Ser
ENST00000502692.5:c.1975A>T ENSP00000422007.1:p.Thr659Ser
ENST00000513398.1:c.1846A>T ENSP00000426797.1:p.Thr616Ser
NM_001104.3:c.1846A>T NP_001095.2:p.Thr616Ser
NM_001258371.2:c.1975A>T NP_001245300.2:p.Thr659Ser
NM_001104.4:c.1846A>T MANE Select NP_001095.2:p.Thr616Ser
NM_001258371.3:c.1975A>T NP_001245300.2:p.Thr659Ser