Canonical Allele Identifier: CA345387528

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236918385T>G (hg19) ; chr1:g.236755085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755085T>G , CM000663.2:g.236755085T>G	GRCh38
NC_000001.10:g.236918385T>G , CM000663.1:g.236918385T>G	GRCh37
NC_000001.9:g.234985008T>G	NCBI36
NG_009081.1:g.73616T>G
NG_009081.2:g.95945T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2041T>G	ENSP00000443495.1:p.Tyr681Asp
ENST00000461367.2:n.337T>G
ENST00000492634.7:n.1971T>G
ENST00000682015.1:c.1948T>G	ENSP00000506961.1:p.Tyr650Asp
ENST00000682692.1:n.3136T>G
ENST00000682966.1:n.7682T>G
ENST00000683111.1:c.*1327T>G	ENSP00000507913.1:n.*1327T>G
ENST00000683322.1:n.3393T>G
ENST00000683805.1:n.832T>G
ENST00000684050.1:n.4679T>G
ENST00000684122.1:n.188T>G
ENST00000684286.1:n.3596T>G
ENST00000684502.1:n.3338T>G
ENST00000684763.1:n.656T>G
ENST00000366578.6:c.2041T>G MANE Select	ENSP00000355537.4:p.Tyr681Asp
ENST00000492634.6:n.1971T>G
ENST00000542672.6:c.2041T>G	ENSP00000443495.1:p.Tyr681Asp
ENST00000651091.1:c.1731T>G	ENSP00000498677.1:n.1731T>G
ENST00000651275.1:c.1933T>G	ENSP00000498926.1:p.Tyr645Asp
ENST00000651781.1:c.1121T>G
ENST00000651786.1:c.*1413T>G	ENSP00000498364.1:n.*1413T>G
ENST00000652096.1:c.*1446T>G	ENSP00000498896.1:n.*1446T>G
ENST00000366578.5:c.2041T>G	ENSP00000355537.4:p.Tyr681Asp
ENST00000461367.1:n.250T>G
ENST00000542672.5:c.2041T>G	ENSP00000443495.1:p.Tyr681Asp
ENST00000546208.5:c.1417T>G	ENSP00000438384.2:p.Tyr473Asp
NM_001103.3:c.2041T>G	NP_001094.1:p.Tyr681Asp
NM_001278343.1:c.2041T>G	NP_001265272.1:p.Tyr681Asp
NM_001278344.1:c.1417T>G	NP_001265273.1:p.Tyr473Asp
NM_001278343.2:c.2041T>G	NP_001265272.1:p.Tyr681Asp
NM_001103.4:c.2041T>G MANE Select	NP_001094.1:p.Tyr681Asp
NM_001278344.2:c.1417T>G	NP_001265273.1:p.Tyr473Asp