Canonical Allele Identifier: CA345387506

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236918374A>T (hg19) ; chr1:g.236755074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755074A>T , CM000663.2:g.236755074A>T	GRCh38
NC_000001.10:g.236918374A>T , CM000663.1:g.236918374A>T	GRCh37
NC_000001.9:g.234984997A>T	NCBI36
NG_009081.1:g.73605A>T
NG_009081.2:g.95934A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2030A>T	ENSP00000443495.1:p.Gln677Leu
ENST00000461367.2:n.326A>T
ENST00000492634.7:n.1960A>T
ENST00000682015.1:c.1937A>T	ENSP00000506961.1:p.Gln646Leu
ENST00000682692.1:n.3125A>T
ENST00000682966.1:n.7671A>T
ENST00000683111.1:c.*1316A>T	ENSP00000507913.1:n.*1316A>T
ENST00000683322.1:n.3382A>T
ENST00000683805.1:n.821A>T
ENST00000684050.1:n.4668A>T
ENST00000684122.1:n.177A>T
ENST00000684286.1:n.3585A>T
ENST00000684502.1:n.3327A>T
ENST00000684763.1:n.645A>T
ENST00000366578.6:c.2030A>T MANE Select	ENSP00000355537.4:p.Gln677Leu
ENST00000492634.6:n.1960A>T
ENST00000542672.6:c.2030A>T	ENSP00000443495.1:p.Gln677Leu
ENST00000651091.1:c.1720A>T	ENSP00000498677.1:n.1720A>T
ENST00000651275.1:c.1922A>T	ENSP00000498926.1:p.Gln641Leu
ENST00000651781.1:c.1110A>T
ENST00000651786.1:c.*1402A>T	ENSP00000498364.1:n.*1402A>T
ENST00000652096.1:c.*1435A>T	ENSP00000498896.1:n.*1435A>T
ENST00000366578.5:c.2030A>T	ENSP00000355537.4:p.Gln677Leu
ENST00000461367.1:n.239A>T
ENST00000542672.5:c.2030A>T	ENSP00000443495.1:p.Gln677Leu
ENST00000546208.5:c.1406A>T	ENSP00000438384.2:p.Gln469Leu
NM_001103.3:c.2030A>T	NP_001094.1:p.Gln677Leu
NM_001278343.1:c.2030A>T	NP_001265272.1:p.Gln677Leu
NM_001278344.1:c.1406A>T	NP_001265273.1:p.Gln469Leu
NM_001278343.2:c.2030A>T	NP_001265272.1:p.Gln677Leu
NM_001103.4:c.2030A>T MANE Select	NP_001094.1:p.Gln677Leu
NM_001278344.2:c.1406A>T	NP_001265273.1:p.Gln469Leu