Canonical Allele Identifier: CA345387744

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236918478C>G (hg19) ; chr1:g.236755178C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755178C>G , CM000663.2:g.236755178C>G	GRCh38
NC_000001.10:g.236918478C>G , CM000663.1:g.236918478C>G	GRCh37
NC_000001.9:g.234985101C>G	NCBI36
NG_009081.1:g.73709C>G
NG_009081.2:g.96038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2134C>G	ENSP00000443495.1:p.His712Asp
ENST00000461367.2:n.430C>G
ENST00000492634.7:n.2064C>G
ENST00000682015.1:c.2041C>G	ENSP00000506961.1:p.His681Asp
ENST00000682692.1:n.3229C>G
ENST00000682966.1:n.7775C>G
ENST00000683111.1:c.*1420C>G	ENSP00000507913.1:n.*1420C>G
ENST00000683322.1:n.3486C>G
ENST00000683805.1:n.925C>G
ENST00000684050.1:n.4772C>G
ENST00000684122.1:n.281C>G
ENST00000684286.1:n.3689C>G
ENST00000684502.1:n.3431C>G
ENST00000684763.1:n.749C>G
ENST00000366578.6:c.2134C>G MANE Select	ENSP00000355537.4:p.His712Asp
ENST00000492634.6:n.2064C>G
ENST00000542672.6:c.2134C>G	ENSP00000443495.1:p.His712Asp
ENST00000651091.1:c.1824C>G	ENSP00000498677.1:n.1824C>G
ENST00000651275.1:c.2026C>G	ENSP00000498926.1:p.His676Asp
ENST00000651781.1:c.1214C>G
ENST00000651786.1:c.*1506C>G	ENSP00000498364.1:n.*1506C>G
ENST00000652096.1:c.*1539C>G	ENSP00000498896.1:n.*1539C>G
ENST00000366578.5:c.2134C>G	ENSP00000355537.4:p.His712Asp
ENST00000461367.1:n.343C>G
ENST00000542672.5:c.2134C>G	ENSP00000443495.1:p.His712Asp
ENST00000546208.5:c.1510C>G	ENSP00000438384.2:p.His504Asp
NM_001103.3:c.2134C>G	NP_001094.1:p.His712Asp
NM_001278343.1:c.2134C>G	NP_001265272.1:p.His712Asp
NM_001278344.1:c.1510C>G	NP_001265273.1:p.His504Asp
NM_001278343.2:c.2134C>G	NP_001265272.1:p.His712Asp
NM_001103.4:c.2134C>G MANE Select	NP_001094.1:p.His712Asp
NM_001278344.2:c.1510C>G	NP_001265273.1:p.His504Asp