Canonical Allele Identifier: CA1144071106
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762501C= , CM000663.2:g.236762501C= GRCh38
NC_000001.10:g.236925801C= , CM000663.1:g.236925801C= GRCh37
NC_000001.9:g.234992424C= NCBI36
NG_009081.1:g.81032C=
NG_009081.2:g.103361C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2567C= ENSP00000443495.1:p.Pro856=
ENST00000461367.2:n.863C=
ENST00000492634.7:n.2497C=
ENST00000682015.1:c.2474C= ENSP00000506961.1:p.Pro825=
ENST00000682490.1:n.485C=
ENST00000682692.1:n.3662C=
ENST00000682966.1:n.8208C=
ENST00000683111.1:c.*1853C= ENSP00000507913.1:n.*1853C=
ENST00000683322.1:n.3919C=
ENST00000683805.1:n.1358C=
ENST00000684050.1:n.5205C=
ENST00000684122.1:n.2001C=
ENST00000684286.1:n.4122C=
ENST00000684502.1:n.3864C=
ENST00000684763.1:n.1182C=
ENST00000366578.6:c.2567C= MANE Select ENSP00000355537.4:p.Pro856=
ENST00000492634.6:n.2497C=
ENST00000542672.6:c.2567C= ENSP00000443495.1:p.Pro856=
ENST00000651091.1:c.2257C= ENSP00000498677.1:n.2257C=
ENST00000651275.1:c.2459C= ENSP00000498926.1:p.Pro820=
ENST00000651781.1:c.1647C=
ENST00000651786.1:c.*1939C= ENSP00000498364.1:n.*1939C=
ENST00000652096.1:c.*1972C= ENSP00000498896.1:n.*1972C=
ENST00000366578.5:c.2567C= ENSP00000355537.4:p.Pro856=
ENST00000461367.1:n.776C=
ENST00000542672.5:c.2567C= ENSP00000443495.1:p.Pro856=
ENST00000546208.5:c.1943C= ENSP00000438384.2:p.Pro648=
NM_001103.3:c.2567C= NP_001094.1:p.Pro856=
NM_001278343.1:c.2567C= NP_001265272.1:p.Pro856=
NM_001278344.1:c.1943C= NP_001265273.1:p.Pro648=
NM_001278343.2:c.2567C= NP_001265272.1:p.Pro856=
NM_001103.4:c.2567C= MANE Select NP_001094.1:p.Pro856=
NM_001278344.2:c.1943C= NP_001265273.1:p.Pro648=