Canonical Allele Identifier: CA345387680

Gene: ACTN2

Linked Data

• gnomAD v4: 1-236755151-C-G
• MyVariant Identifiers: chr1:g.236918451C>G (hg19) ; chr1:g.236755151C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236755151C>G , CM000663.2:g.236755151C>G	GRCh38
NC_000001.10:g.236918451C>G , CM000663.1:g.236918451C>G	GRCh37
NC_000001.9:g.234985074C>G	NCBI36
NG_009081.1:g.73682C>G
NG_009081.2:g.96011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2107C>G	ENSP00000443495.1:p.Gln703Glu
ENST00000461367.2:n.403C>G
ENST00000492634.7:n.2037C>G
ENST00000682015.1:c.2014C>G	ENSP00000506961.1:p.Gln672Glu
ENST00000682692.1:n.3202C>G
ENST00000682966.1:n.7748C>G
ENST00000683111.1:c.*1393C>G	ENSP00000507913.1:n.*1393C>G
ENST00000683322.1:n.3459C>G
ENST00000683805.1:n.898C>G
ENST00000684050.1:n.4745C>G
ENST00000684122.1:n.254C>G
ENST00000684286.1:n.3662C>G
ENST00000684502.1:n.3404C>G
ENST00000684763.1:n.722C>G
ENST00000366578.6:c.2107C>G MANE Select	ENSP00000355537.4:p.Gln703Glu
ENST00000492634.6:n.2037C>G
ENST00000542672.6:c.2107C>G	ENSP00000443495.1:p.Gln703Glu
ENST00000651091.1:c.1797C>G	ENSP00000498677.1:n.1797C>G
ENST00000651275.1:c.1999C>G	ENSP00000498926.1:p.Gln667Glu
ENST00000651781.1:c.1187C>G
ENST00000651786.1:c.*1479C>G	ENSP00000498364.1:n.*1479C>G
ENST00000652096.1:c.*1512C>G	ENSP00000498896.1:n.*1512C>G
ENST00000366578.5:c.2107C>G	ENSP00000355537.4:p.Gln703Glu
ENST00000461367.1:n.316C>G
ENST00000542672.5:c.2107C>G	ENSP00000443495.1:p.Gln703Glu
ENST00000546208.5:c.1483C>G	ENSP00000438384.2:p.Gln495Glu
NM_001103.3:c.2107C>G	NP_001094.1:p.Gln703Glu
NM_001278343.1:c.2107C>G	NP_001265272.1:p.Gln703Glu
NM_001278344.1:c.1483C>G	NP_001265273.1:p.Gln495Glu
NM_001278343.2:c.2107C>G	NP_001265272.1:p.Gln703Glu
NM_001103.4:c.2107C>G MANE Select	NP_001094.1:p.Gln703Glu
NM_001278344.2:c.1483C>G	NP_001265273.1:p.Gln495Glu