Canonical Allele Identifier: CA345373453

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882197A>T (hg19) ; chr1:g.236718897A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718897A>T , CM000663.2:g.236718897A>T	GRCh38
NC_000001.10:g.236882197A>T , CM000663.1:g.236882197A>T	GRCh37
NC_000001.9:g.234948820A>T	NCBI36
NG_009081.1:g.37428A>T
NG_009081.2:g.59757A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.245A>T	ENSP00000443495.1:p.Glu82Val
ENST00000492634.7:n.340A>T
ENST00000682015.1:c.245A>T	ENSP00000506961.1:p.Glu82Val
ENST00000682692.1:n.245A>T
ENST00000682966.1:n.244A>T
ENST00000683075.1:n.184A>T
ENST00000683111.1:c.188A>T	ENSP00000507913.1:p.Glu63Val
ENST00000684050.1:n.280A>T
ENST00000684286.1:n.313A>T
ENST00000684502.1:n.280A>T
ENST00000366578.6:c.245A>T MANE Select	ENSP00000355537.4:p.Glu82Val
ENST00000492634.6:n.340A>T
ENST00000542672.6:c.245A>T	ENSP00000443495.1:p.Glu82Val
ENST00000651091.1:c.188A>T	ENSP00000498677.1:p.Glu63Val
ENST00000651187.1:c.29A>T	ENSP00000498348.1:p.Glu10Val
ENST00000651275.1:c.230A>T	ENSP00000498926.1:p.Glu77Val
ENST00000651786.1:c.245A>T	ENSP00000498364.1:p.Glu82Val
ENST00000652096.1:c.245A>T	ENSP00000498896.1:p.Glu82Val
ENST00000366578.5:c.245A>T	ENSP00000355537.4:p.Glu82Val
ENST00000492634.5:n.392A>T
ENST00000542672.5:c.245A>T	ENSP00000443495.1:p.Glu82Val
ENST00000546208.5:c.-577A>T	ENSP00000438384.2:n.-577A>T
NM_001103.3:c.245A>T	NP_001094.1:p.Glu82Val
NM_001278343.1:c.245A>T	NP_001265272.1:p.Glu82Val
NM_001278344.1:c.-577A>T	NP_001265273.1:n.-577A>T
NM_001278343.2:c.245A>T	NP_001265272.1:p.Glu82Val
NM_001103.4:c.245A>T MANE Select	NP_001094.1:p.Glu82Val
NM_001278344.2:c.-577A>T	NP_001265273.1:n.-577A>T