Canonical Allele Identifier: CA345386911

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236917331T>A (hg19) ; chr1:g.236754031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236754031T>A , CM000663.2:g.236754031T>A	GRCh38
NC_000001.10:g.236917331T>A , CM000663.1:g.236917331T>A	GRCh37
NC_000001.9:g.234983954T>A	NCBI36
NG_009081.1:g.72562T>A
NG_009081.2:g.94891T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.1924T>A	ENSP00000443495.1:p.Phe642Ile
ENST00000461367.2:n.220T>A
ENST00000492634.7:n.1854T>A
ENST00000682015.1:c.1831T>A	ENSP00000506961.1:p.Phe611Ile
ENST00000682692.1:n.3019T>A
ENST00000682966.1:n.7565T>A
ENST00000683111.1:c.*1210T>A	ENSP00000507913.1:n.*1210T>A
ENST00000683322.1:n.3276T>A
ENST00000684050.1:n.4562T>A
ENST00000684286.1:n.3479T>A
ENST00000684502.1:n.3221T>A
ENST00000684763.1:n.539T>A
ENST00000366578.6:c.1924T>A MANE Select	ENSP00000355537.4:p.Phe642Ile
ENST00000492634.6:n.1854T>A
ENST00000542672.6:c.1924T>A	ENSP00000443495.1:p.Phe642Ile
ENST00000651091.1:c.1614T>A	ENSP00000498677.1:n.1614T>A
ENST00000651275.1:c.1816T>A	ENSP00000498926.1:p.Phe606Ile
ENST00000651781.1:c.1004T>A
ENST00000651786.1:c.*1296T>A	ENSP00000498364.1:n.*1296T>A
ENST00000652096.1:c.*1329T>A	ENSP00000498896.1:n.*1329T>A
ENST00000366578.5:c.1924T>A	ENSP00000355537.4:p.Phe642Ile
ENST00000461367.1:n.133T>A
ENST00000542672.5:c.1924T>A	ENSP00000443495.1:p.Phe642Ile
ENST00000546208.5:c.1300T>A	ENSP00000438384.2:p.Phe434Ile
NM_001103.3:c.1924T>A	NP_001094.1:p.Phe642Ile
NM_001278343.1:c.1924T>A	NP_001265272.1:p.Phe642Ile
NM_001278344.1:c.1300T>A	NP_001265273.1:p.Phe434Ile
NM_001278343.2:c.1924T>A	NP_001265272.1:p.Phe642Ile
NM_001103.4:c.1924T>A MANE Select	NP_001094.1:p.Phe642Ile
NM_001278344.2:c.1300T>A	NP_001265273.1:p.Phe434Ile