Canonical Allele Identifier: CA345392334

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925830A>G (hg19) ; chr1:g.236762530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762530A>G , CM000663.2:g.236762530A>G	GRCh38
NC_000001.10:g.236925830A>G , CM000663.1:g.236925830A>G	GRCh37
NC_000001.9:g.234992453A>G	NCBI36
NG_009081.1:g.81061A>G
NG_009081.2:g.103390A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2596A>G	ENSP00000443495.1:p.Met866Val
ENST00000461367.2:n.892A>G
ENST00000492634.7:n.2526A>G
ENST00000682015.1:c.2503A>G	ENSP00000506961.1:p.Met835Val
ENST00000682490.1:n.514A>G
ENST00000682692.1:n.3691A>G
ENST00000682966.1:n.8237A>G
ENST00000683111.1:c.*1882A>G	ENSP00000507913.1:n.*1882A>G
ENST00000683322.1:n.3948A>G
ENST00000683805.1:n.1387A>G
ENST00000684050.1:n.5234A>G
ENST00000684122.1:n.2030A>G
ENST00000684286.1:n.4151A>G
ENST00000684502.1:n.3893A>G
ENST00000684763.1:n.1211A>G
ENST00000366578.6:c.2596A>G MANE Select	ENSP00000355537.4:p.Met866Val
ENST00000492634.6:n.2526A>G
ENST00000542672.6:c.2596A>G	ENSP00000443495.1:p.Met866Val
ENST00000651091.1:c.2286A>G	ENSP00000498677.1:n.2286A>G
ENST00000651275.1:c.2488A>G	ENSP00000498926.1:p.Met830Val
ENST00000651781.1:c.1676A>G
ENST00000651786.1:c.*1968A>G	ENSP00000498364.1:n.*1968A>G
ENST00000652096.1:c.*2001A>G	ENSP00000498896.1:n.*2001A>G
ENST00000366578.5:c.2596A>G	ENSP00000355537.4:p.Met866Val
ENST00000461367.1:n.805A>G
ENST00000542672.5:c.2596A>G	ENSP00000443495.1:p.Met866Val
ENST00000546208.5:c.1972A>G	ENSP00000438384.2:p.Met658Val
NM_001103.3:c.2596A>G	NP_001094.1:p.Met866Val
NM_001278343.1:c.2596A>G	NP_001265272.1:p.Met866Val
NM_001278344.1:c.1972A>G	NP_001265273.1:p.Met658Val
NM_001278343.2:c.2596A>G	NP_001265272.1:p.Met866Val
NM_001103.4:c.2596A>G MANE Select	NP_001094.1:p.Met866Val
NM_001278344.2:c.1972A>G	NP_001265273.1:p.Met658Val