Canonical Allele Identifier: CA1144229255
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762521A= , CM000663.2:g.236762521A= GRCh38
NC_000001.10:g.236925821A= , CM000663.1:g.236925821A= GRCh37
NC_000001.9:g.234992444A= NCBI36
NG_009081.1:g.81052A=
NG_009081.2:g.103381A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2587A= ENSP00000443495.1:p.Ile863=
ENST00000461367.2:n.883A=
ENST00000492634.7:n.2517A=
ENST00000682015.1:c.2494A= ENSP00000506961.1:p.Ile832=
ENST00000682490.1:n.505A=
ENST00000682692.1:n.3682A=
ENST00000682966.1:n.8228A=
ENST00000683111.1:c.*1873A= ENSP00000507913.1:n.*1873A=
ENST00000683322.1:n.3939A=
ENST00000683805.1:n.1378A=
ENST00000684050.1:n.5225A=
ENST00000684122.1:n.2021A=
ENST00000684286.1:n.4142A=
ENST00000684502.1:n.3884A=
ENST00000684763.1:n.1202A=
ENST00000366578.6:c.2587A= MANE Select ENSP00000355537.4:p.Ile863=
ENST00000492634.6:n.2517A=
ENST00000542672.6:c.2587A= ENSP00000443495.1:p.Ile863=
ENST00000651091.1:c.2277A= ENSP00000498677.1:n.2277A=
ENST00000651275.1:c.2479A= ENSP00000498926.1:p.Ile827=
ENST00000651781.1:c.1667A=
ENST00000651786.1:c.*1959A= ENSP00000498364.1:n.*1959A=
ENST00000652096.1:c.*1992A= ENSP00000498896.1:n.*1992A=
ENST00000366578.5:c.2587A= ENSP00000355537.4:p.Ile863=
ENST00000461367.1:n.796A=
ENST00000542672.5:c.2587A= ENSP00000443495.1:p.Ile863=
ENST00000546208.5:c.1963A= ENSP00000438384.2:p.Ile655=
NM_001103.3:c.2587A= NP_001094.1:p.Ile863=
NM_001278343.1:c.2587A= NP_001265272.1:p.Ile863=
NM_001278344.1:c.1963A= NP_001265273.1:p.Ile655=
NM_001278343.2:c.2587A= NP_001265272.1:p.Ile863=
NM_001103.4:c.2587A= MANE Select NP_001094.1:p.Ile863=
NM_001278344.2:c.1963A= NP_001265273.1:p.Ile655=