Canonical Allele Identifier: CA1141679730

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718896G= , CM000663.2:g.236718896G=	GRCh38
NC_000001.10:g.236882196G= , CM000663.1:g.236882196G=	GRCh37
NC_000001.9:g.234948819G=	NCBI36
NG_009081.1:g.37427G=
NG_009081.2:g.59756G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.244G=	ENSP00000443495.1:p.Glu82=
ENST00000492634.7:n.339G=
ENST00000682015.1:c.244G=	ENSP00000506961.1:p.Glu82=
ENST00000682692.1:n.244G=
ENST00000682966.1:n.243G=
ENST00000683075.1:n.183G=
ENST00000683111.1:c.187G=	ENSP00000507913.1:p.Glu63=
ENST00000684050.1:n.279G=
ENST00000684286.1:n.312G=
ENST00000684502.1:n.279G=
ENST00000366578.6:c.244G= MANE Select	ENSP00000355537.4:p.Glu82=
ENST00000492634.6:n.339G=
ENST00000542672.6:c.244G=	ENSP00000443495.1:p.Glu82=
ENST00000651091.1:c.187G=	ENSP00000498677.1:p.Glu63=
ENST00000651187.1:c.28G=	ENSP00000498348.1:p.Glu10=
ENST00000651275.1:c.229G=	ENSP00000498926.1:p.Glu77=
ENST00000651786.1:c.244G=	ENSP00000498364.1:p.Glu82=
ENST00000652096.1:c.244G=	ENSP00000498896.1:p.Glu82=
ENST00000366578.5:c.244G=	ENSP00000355537.4:p.Glu82=
ENST00000492634.5:n.391G=
ENST00000542672.5:c.244G=	ENSP00000443495.1:p.Glu82=
ENST00000546208.5:c.-578G=	ENSP00000438384.2:n.-578G=
NM_001103.3:c.244G=	NP_001094.1:p.Glu82=
NM_001278343.1:c.244G=	NP_001265272.1:p.Glu82=
NM_001278344.1:c.-578G=	NP_001265273.1:n.-578G=
NM_001278343.2:c.244G=	NP_001265272.1:p.Glu82=
NM_001103.4:c.244G= MANE Select	NP_001094.1:p.Glu82=
NM_001278344.2:c.-578G=	NP_001265273.1:n.-578G=