Canonical Allele Identifier: CA2487053235

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762587T= , CM000663.2:g.236762587T=	GRCh38
NC_000001.10:g.236925887T= , CM000663.1:g.236925887T=	GRCh37
NC_000001.9:g.234992510T=	NCBI36
NG_009081.1:g.81118T=
NG_009081.2:g.103447T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2653T=	ENSP00000443495.1:p.Ser885=
ENST00000461367.2:n.949T=
ENST00000492634.7:n.2583T=
ENST00000682015.1:c.2560T=	ENSP00000506961.1:p.Ser854=
ENST00000682490.1:n.571T=
ENST00000682692.1:n.3748T=
ENST00000682966.1:n.8294T=
ENST00000683111.1:c.*1939T=	ENSP00000507913.1:n.*1939T=
ENST00000683322.1:n.4005T=
ENST00000683805.1:n.1444T=
ENST00000684050.1:n.5291T=
ENST00000684122.1:n.2087T=
ENST00000684286.1:n.4208T=
ENST00000684502.1:n.3950T=
ENST00000684763.1:n.1268T=
ENST00000366578.6:c.2653T= MANE Select	ENSP00000355537.4:p.Ser885=
ENST00000492634.6:n.2583T=
ENST00000542672.6:c.2653T=	ENSP00000443495.1:p.Ser885=
ENST00000651091.1:c.2343T=	ENSP00000498677.1:n.2343T=
ENST00000651275.1:c.2545T=	ENSP00000498926.1:p.Ser849=
ENST00000651781.1:c.1733T=
ENST00000651786.1:c.*2025T=	ENSP00000498364.1:n.*2025T=
ENST00000652096.1:c.*2058T=	ENSP00000498896.1:n.*2058T=
ENST00000366578.5:c.2653T=	ENSP00000355537.4:p.Ser885=
ENST00000542672.5:c.2653T=	ENSP00000443495.1:p.Ser885=
ENST00000546208.5:c.2029T=	ENSP00000438384.2:p.Ser677=
NM_001103.3:c.2653T=	NP_001094.1:p.Ser885=
NM_001278343.1:c.2653T=	NP_001265272.1:p.Ser885=
NM_001278344.1:c.2029T=	NP_001265273.1:p.Ser677=
NM_001278343.2:c.2653T=	NP_001265272.1:p.Ser885=
NM_001103.4:c.2653T= MANE Select	NP_001094.1:p.Ser885=
NM_001278344.2:c.2029T=	NP_001265273.1:p.Ser677=