Canonical Allele Identifier: CA1013665155

Gene: ACTN2

Linked Data

• gnomAD v3: 1-236762720-G-A
• gnomAD v4: 1-236762720-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762720G>A , CM000663.2:g.236762720G>A	GRCh38
NC_000001.10:g.236926020G>A , CM000663.1:g.236926020G>A	GRCh37
NC_000001.9:g.234992643G>A	NCBI36
NG_009081.1:g.81251G>A
NG_009081.2:g.103580G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.*101G>A	ENSP00000443495.1:n.*101G>A
ENST00000461367.2:n.1082G>A
ENST00000492634.7:n.2716G>A
ENST00000682015.1:c.*101G>A	ENSP00000506961.1:n.*101G>A
ENST00000682490.1:n.704G>A
ENST00000682692.1:n.3881G>A
ENST00000682966.1:n.8427G>A
ENST00000683111.1:c.*2072G>A	ENSP00000507913.1:n.*2072G>A
ENST00000683322.1:n.4138G>A
ENST00000683805.1:n.1577G>A
ENST00000684050.1:n.5424G>A
ENST00000684122.1:n.2220G>A
ENST00000684286.1:n.4341G>A
ENST00000684502.1:n.4083G>A
ENST00000684763.1:n.1401G>A
ENST00000366578.6:c.*101G>A MANE Select	ENSP00000355537.4:n.*101G>A
ENST00000492634.6:n.2716G>A
ENST00000542672.6:c.*101G>A	ENSP00000443495.1:n.*101G>A
ENST00000651275.1:c.2678G>A	ENSP00000498926.1:n.2678G>A
ENST00000651781.1:c.1866G>A
ENST00000652096.1:c.*2191G>A	ENSP00000498896.1:n.*2191G>A
ENST00000366578.5:c.*101G>A	ENSP00000355537.4:n.*101G>A
ENST00000542672.5:c.*101G>A	ENSP00000443495.1:n.*101G>A
ENST00000546208.5:c.*101G>A	ENSP00000438384.2:n.*101G>A
NM_001103.3:c.*101G>A	NP_001094.1:n.*101G>A
NM_001278343.1:c.*101G>A	NP_001265272.1:n.*101G>A
NM_001278344.1:c.*101G>A	NP_001265273.1:n.*101G>A
NM_001278343.2:c.*101G>A	NP_001265272.1:n.*101G>A
NM_001103.4:c.*101G>A MANE Select	NP_001094.1:n.*101G>A
NM_001278344.2:c.*101G>A	NP_001265273.1:n.*101G>A