Canonical Allele Identifier: CA2487049936

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236754094_236754106delinsCCTCCCAGGCGCT , CM000663.2:g.236754094_236754106delinsCCTCCCAGGCGCT	GRCh38
NC_000001.10:g.236917394_236917406delinsCCTCCCAGGCGCT , CM000663.1:g.236917394_236917406delinsCCTCCCAGGCGCT	GRCh37
NC_000001.9:g.234984017_234984029delinsCCTCCCAGGCGCT	NCBI36
NG_009081.1:g.72625_72637delinsCCTCCCAGGCGCT
NG_009081.2:g.94954_94966delinsCCTCCCAGGCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.1974+13_1974+25delinsCCTCCCAGGCGCT	ENSP00000443495.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
ENST00000461367.2:n.270+13_270+25delinsCCTCCCAGGCGCT
ENST00000492634.7:n.1904+13_1904+25delinsCCTCCCAGGCGCT
ENST00000682015.1:c.1881+13_1881+25delinsCCTCCCAGGCGCT	ENSP00000506961.1:n.1881+13_1881+25delinsCCTCCCAGGCGCT
ENST00000682692.1:n.3069+13_3069+25delinsCCTCCCAGGCGCT
ENST00000682966.1:n.7615+13_7615+25delinsCCTCCCAGGCGCT
ENST00000683111.1:c.*1260+13_*1260+25delinsCCTCCCAGGCGCT	ENSP00000507913.1:n.*1260+13_*1260+25delinsCCTCCCAGGCGCT
ENST00000683322.1:n.3326+13_3326+25delinsCCTCCCAGGCGCT
ENST00000684050.1:n.4612+13_4612+25delinsCCTCCCAGGCGCT
ENST00000684286.1:n.3529+13_3529+25delinsCCTCCCAGGCGCT
ENST00000684502.1:n.3271+13_3271+25delinsCCTCCCAGGCGCT
ENST00000684763.1:n.589+13_589+25delinsCCTCCCAGGCGCT
ENST00000366578.6:c.1974+13_1974+25delinsCCTCCCAGGCGCT MANE Select	ENSP00000355537.4:n.1974+13_1974+25delinsCCTCCCAGGCGCT
ENST00000492634.6:n.1904+13_1904+25delinsCCTCCCAGGCGCT
ENST00000542672.6:c.1974+13_1974+25delinsCCTCCCAGGCGCT	ENSP00000443495.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
ENST00000651091.1:c.1664+13_1664+25delinsCCTCCCAGGCGCT	ENSP00000498677.1:n.1664+13_1664+25delinsCCTCCCAGGCGCT
ENST00000651275.1:c.1866+13_1866+25delinsCCTCCCAGGCGCT	ENSP00000498926.1:n.1866+13_1866+25delinsCCTCCCAGGCGCT
ENST00000651781.1:c.1054+13_1054+25delinsCCTCCCAGGCGCT
ENST00000651786.1:c.*1346+13_*1346+25delinsCCTCCCAGGCGCT	ENSP00000498364.1:n.*1346+13_*1346+25delinsCCTCCCAGGCGCT
ENST00000652096.1:c.*1379+13_*1379+25delinsCCTCCCAGGCGCT	ENSP00000498896.1:n.*1379+13_*1379+25delinsCCTCCCAGGCGCT
ENST00000366578.5:c.1974+13_1974+25delinsCCTCCCAGGCGCT	ENSP00000355537.4:n.1974+13_1974+25delinsCCTCCCAGGCGCT
ENST00000461367.1:n.183+13_183+25delinsCCTCCCAGGCGCT
ENST00000542672.5:c.1974+13_1974+25delinsCCTCCCAGGCGCT	ENSP00000443495.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
ENST00000546208.5:c.1350+13_1350+25delinsCCTCCCAGGCGCT	ENSP00000438384.2:n.1350+13_1350+25delinsCCTCCCAGGCGCT
NM_001103.3:c.1974+13_1974+25delinsCCTCCCAGGCGCT	NP_001094.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
NM_001278343.1:c.1974+13_1974+25delinsCCTCCCAGGCGCT	NP_001265272.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
NM_001278344.1:c.1350+13_1350+25delinsCCTCCCAGGCGCT	NP_001265273.1:n.1350+13_1350+25delinsCCTCCCAGGCGCT
NM_001278343.2:c.1974+13_1974+25delinsCCTCCCAGGCGCT	NP_001265272.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
NM_001103.4:c.1974+13_1974+25delinsCCTCCCAGGCGCT MANE Select	NP_001094.1:n.1974+13_1974+25delinsCCTCCCAGGCGCT
NM_001278344.2:c.1350+13_1350+25delinsCCTCCCAGGCGCT	NP_001265273.1:n.1350+13_1350+25delinsCCTCCCAGGCGCT