Canonical Allele Identifier: CA381446788
Gene: ACTN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560306A>T , CM000673.2:g.66560306A>T GRCh38
NC_000011.9:g.66327777A>T , CM000673.1:g.66327777A>T GRCh37
NC_000011.8:g.66084353A>T NCBI36
NG_013304.2:g.18387A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1672A>T MANE Select ENSP00000426797.1:p.Thr558Ser
ENST00000502692.5:c.1801A>T ENSP00000422007.1:p.Thr601Ser
ENST00000513398.1:c.1672A>T ENSP00000426797.1:p.Thr558Ser
NM_001104.3:c.1672A>T NP_001095.2:p.Thr558Ser
NM_001258371.2:c.1801A>T NP_001245300.2:p.Thr601Ser
NM_001104.4:c.1672A>T MANE Select NP_001095.2:p.Thr558Ser
NM_001258371.3:c.1801A>T NP_001245300.2:p.Thr601Ser