Canonical Allele Identifier: CA345392163

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925798C>G (hg19) ; chr1:g.236762498C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762498C>G , CM000663.2:g.236762498C>G	GRCh38
NC_000001.10:g.236925798C>G , CM000663.1:g.236925798C>G	GRCh37
NC_000001.9:g.234992421C>G	NCBI36
NG_009081.1:g.81029C>G
NG_009081.2:g.103358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2564C>G	ENSP00000443495.1:p.Pro855Arg
ENST00000461367.2:n.860C>G
ENST00000492634.7:n.2494C>G
ENST00000682015.1:c.2471C>G	ENSP00000506961.1:p.Pro824Arg
ENST00000682490.1:n.482C>G
ENST00000682692.1:n.3659C>G
ENST00000682966.1:n.8205C>G
ENST00000683111.1:c.*1850C>G	ENSP00000507913.1:n.*1850C>G
ENST00000683322.1:n.3916C>G
ENST00000683805.1:n.1355C>G
ENST00000684050.1:n.5202C>G
ENST00000684122.1:n.1998C>G
ENST00000684286.1:n.4119C>G
ENST00000684502.1:n.3861C>G
ENST00000684763.1:n.1179C>G
ENST00000366578.6:c.2564C>G MANE Select	ENSP00000355537.4:p.Pro855Arg
ENST00000492634.6:n.2494C>G
ENST00000542672.6:c.2564C>G	ENSP00000443495.1:p.Pro855Arg
ENST00000651091.1:c.2254C>G	ENSP00000498677.1:n.2254C>G
ENST00000651275.1:c.2456C>G	ENSP00000498926.1:p.Pro819Arg
ENST00000651781.1:c.1644C>G
ENST00000651786.1:c.*1936C>G	ENSP00000498364.1:n.*1936C>G
ENST00000652096.1:c.*1969C>G	ENSP00000498896.1:n.*1969C>G
ENST00000366578.5:c.2564C>G	ENSP00000355537.4:p.Pro855Arg
ENST00000461367.1:n.773C>G
ENST00000542672.5:c.2564C>G	ENSP00000443495.1:p.Pro855Arg
ENST00000546208.5:c.1940C>G	ENSP00000438384.2:p.Pro647Arg
NM_001103.3:c.2564C>G	NP_001094.1:p.Pro855Arg
NM_001278343.1:c.2564C>G	NP_001265272.1:p.Pro855Arg
NM_001278344.1:c.1940C>G	NP_001265273.1:p.Pro647Arg
NM_001278343.2:c.2564C>G	NP_001265272.1:p.Pro855Arg
NM_001103.4:c.2564C>G MANE Select	NP_001094.1:p.Pro855Arg
NM_001278344.2:c.1940C>G	NP_001265273.1:p.Pro647Arg