Canonical Allele Identifier: CA2487053211
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762541C= , CM000663.2:g.236762541C= GRCh38
NC_000001.10:g.236925841C= , CM000663.1:g.236925841C= GRCh37
NC_000001.9:g.234992464C= NCBI36
NG_009081.1:g.81072C=
NG_009081.2:g.103401C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2607C= ENSP00000443495.1:p.Tyr869=
ENST00000461367.2:n.903C=
ENST00000492634.7:n.2537C=
ENST00000682015.1:c.2514C= ENSP00000506961.1:p.Tyr838=
ENST00000682490.1:n.525C=
ENST00000682692.1:n.3702C=
ENST00000682966.1:n.8248C=
ENST00000683111.1:c.*1893C= ENSP00000507913.1:n.*1893C=
ENST00000683322.1:n.3959C=
ENST00000683805.1:n.1398C=
ENST00000684050.1:n.5245C=
ENST00000684122.1:n.2041C=
ENST00000684286.1:n.4162C=
ENST00000684502.1:n.3904C=
ENST00000684763.1:n.1222C=
ENST00000366578.6:c.2607C= MANE Select ENSP00000355537.4:p.Tyr869=
ENST00000492634.6:n.2537C=
ENST00000542672.6:c.2607C= ENSP00000443495.1:p.Tyr869=
ENST00000651091.1:c.2297C= ENSP00000498677.1:n.2297C=
ENST00000651275.1:c.2499C= ENSP00000498926.1:p.Tyr833=
ENST00000651781.1:c.1687C=
ENST00000651786.1:c.*1979C= ENSP00000498364.1:n.*1979C=
ENST00000652096.1:c.*2012C= ENSP00000498896.1:n.*2012C=
ENST00000366578.5:c.2607C= ENSP00000355537.4:p.Tyr869=
ENST00000461367.1:n.816C=
ENST00000542672.5:c.2607C= ENSP00000443495.1:p.Tyr869=
ENST00000546208.5:c.1983C= ENSP00000438384.2:p.Tyr661=
NM_001103.3:c.2607C= NP_001094.1:p.Tyr869=
NM_001278343.1:c.2607C= NP_001265272.1:p.Tyr869=
NM_001278344.1:c.1983C= NP_001265273.1:p.Tyr661=
NM_001278343.2:c.2607C= NP_001265272.1:p.Tyr869=
NM_001103.4:c.2607C= MANE Select NP_001094.1:p.Tyr869=
NM_001278344.2:c.1983C= NP_001265273.1:p.Tyr661=