Canonical Allele Identifier: CA345392357

Gene: ACTN2

Linked Data

• dbSNP Id: rs1659739403
• MyVariant Identifiers: chr1:g.236925833C>A (hg19) ; chr1:g.236762533C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762533C>A , CM000663.2:g.236762533C>A	GRCh38
NC_000001.10:g.236925833C>A , CM000663.1:g.236925833C>A	GRCh37
NC_000001.9:g.234992456C>A	NCBI36
NG_009081.1:g.81064C>A
NG_009081.2:g.103393C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2599C>A	ENSP00000443495.1:p.Pro867Thr
ENST00000461367.2:n.895C>A
ENST00000492634.7:n.2529C>A
ENST00000682015.1:c.2506C>A	ENSP00000506961.1:p.Pro836Thr
ENST00000682490.1:n.517C>A
ENST00000682692.1:n.3694C>A
ENST00000682966.1:n.8240C>A
ENST00000683111.1:c.*1885C>A	ENSP00000507913.1:n.*1885C>A
ENST00000683322.1:n.3951C>A
ENST00000683805.1:n.1390C>A
ENST00000684050.1:n.5237C>A
ENST00000684122.1:n.2033C>A
ENST00000684286.1:n.4154C>A
ENST00000684502.1:n.3896C>A
ENST00000684763.1:n.1214C>A
ENST00000366578.6:c.2599C>A MANE Select	ENSP00000355537.4:p.Pro867Thr
ENST00000492634.6:n.2529C>A
ENST00000542672.6:c.2599C>A	ENSP00000443495.1:p.Pro867Thr
ENST00000651091.1:c.2289C>A	ENSP00000498677.1:n.2289C>A
ENST00000651275.1:c.2491C>A	ENSP00000498926.1:p.Pro831Thr
ENST00000651781.1:c.1679C>A
ENST00000651786.1:c.*1971C>A	ENSP00000498364.1:n.*1971C>A
ENST00000652096.1:c.*2004C>A	ENSP00000498896.1:n.*2004C>A
ENST00000366578.5:c.2599C>A	ENSP00000355537.4:p.Pro867Thr
ENST00000461367.1:n.808C>A
ENST00000542672.5:c.2599C>A	ENSP00000443495.1:p.Pro867Thr
ENST00000546208.5:c.1975C>A	ENSP00000438384.2:p.Pro659Thr
NM_001103.3:c.2599C>A	NP_001094.1:p.Pro867Thr
NM_001278343.1:c.2599C>A	NP_001265272.1:p.Pro867Thr
NM_001278344.1:c.1975C>A	NP_001265273.1:p.Pro659Thr
NM_001278343.2:c.2599C>A	NP_001265272.1:p.Pro867Thr
NM_001103.4:c.2599C>A MANE Select	NP_001094.1:p.Pro867Thr
NM_001278344.2:c.1975C>A	NP_001265273.1:p.Pro659Thr