Canonical Allele Identifier: CA1148265782

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762422T= , CM000663.2:g.236762422T=	GRCh38
NC_000001.10:g.236925722T= , CM000663.1:g.236925722T=	GRCh37
NC_000001.9:g.234992345T=	NCBI36
NG_009081.1:g.80953T=
NG_009081.2:g.103282T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2527-39T=	ENSP00000443495.1:n.2527-39T=
ENST00000461367.2:n.823-39T=
ENST00000492634.7:n.2457-39T=
ENST00000682015.1:c.2434-39T=	ENSP00000506961.1:n.2434-39T=
ENST00000682490.1:n.445-39T=
ENST00000682692.1:n.3622-39T=
ENST00000682966.1:n.8168-39T=
ENST00000683111.1:c.*1813-39T=	ENSP00000507913.1:n.*1813-39T=
ENST00000683322.1:n.3879-39T=
ENST00000683805.1:n.1318-39T=
ENST00000684050.1:n.5165-39T=
ENST00000684122.1:n.1922T=
ENST00000684286.1:n.4082-39T=
ENST00000684502.1:n.3824-39T=
ENST00000684763.1:n.1142-39T=
ENST00000366578.6:c.2527-39T= MANE Select	ENSP00000355537.4:n.2527-39T=
ENST00000492634.6:n.2457-39T=
ENST00000542672.6:c.2527-39T=	ENSP00000443495.1:n.2527-39T=
ENST00000651091.1:c.2217-39T=	ENSP00000498677.1:n.2217-39T=
ENST00000651275.1:c.2419-39T=	ENSP00000498926.1:n.2419-39T=
ENST00000651781.1:c.1607-39T=
ENST00000651786.1:c.*1899-39T=	ENSP00000498364.1:n.*1899-39T=
ENST00000652096.1:c.*1932-39T=	ENSP00000498896.1:n.*1932-39T=
ENST00000366578.5:c.2527-39T=	ENSP00000355537.4:n.2527-39T=
ENST00000461367.1:n.736-39T=
ENST00000542672.5:c.2527-39T=	ENSP00000443495.1:n.2527-39T=
ENST00000546208.5:c.1903-39T=	ENSP00000438384.2:n.1903-39T=
NM_001103.3:c.2527-39T=	NP_001094.1:n.2527-39T=
NM_001278343.1:c.2527-39T=	NP_001265272.1:n.2527-39T=
NM_001278344.1:c.1903-39T=	NP_001265273.1:n.1903-39T=
NM_001278343.2:c.2527-39T=	NP_001265272.1:n.2527-39T=
NM_001103.4:c.2527-39T= MANE Select	NP_001094.1:n.2527-39T=
NM_001278344.2:c.1903-39T=	NP_001265273.1:n.1903-39T=