Canonical Allele Identifier: CA2487051215
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236757510C= , CM000663.2:g.236757510C= GRCh38
NC_000001.10:g.236920810C= , CM000663.1:g.236920810C= GRCh37
NC_000001.9:g.234987433C= NCBI36
NG_009081.1:g.76041C=
NG_009081.2:g.98370C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542672.7:c.2179C= ENSP00000443495.1:p.Leu727=
ENST00000461367.2:n.475C=
ENST00000492634.7:n.2109C=
ENST00000682015.1:c.2086C= ENSP00000506961.1:p.Leu696=
ENST00000682490.1:n.97C=
ENST00000682692.1:n.3274C=
ENST00000682966.1:n.7820C=
ENST00000683111.1:c.*1465C= ENSP00000507913.1:n.*1465C=
ENST00000683322.1:n.3531C=
ENST00000683805.1:n.970C=
ENST00000684050.1:n.4817C=
ENST00000684122.1:n.326C=
ENST00000684286.1:n.3734C=
ENST00000684502.1:n.3476C=
ENST00000684763.1:n.794C=
ENST00000366578.6:c.2179C= MANE Select ENSP00000355537.4:p.Leu727=
ENST00000492634.6:n.2109C=
ENST00000542672.6:c.2179C= ENSP00000443495.1:p.Leu727=
ENST00000651091.1:c.1869C= ENSP00000498677.1:n.1869C=
ENST00000651275.1:c.2071C= ENSP00000498926.1:p.Leu691=
ENST00000651781.1:c.1259C=
ENST00000651786.1:c.*1551C= ENSP00000498364.1:n.*1551C=
ENST00000652096.1:c.*1584C= ENSP00000498896.1:n.*1584C=
ENST00000366578.5:c.2179C= ENSP00000355537.4:p.Leu727=
ENST00000461367.1:n.388C=
ENST00000542672.5:c.2179C= ENSP00000443495.1:p.Leu727=
ENST00000546208.5:c.1555C= ENSP00000438384.2:p.Leu519=
NM_001103.3:c.2179C= NP_001094.1:p.Leu727=
NM_001278343.1:c.2179C= NP_001265272.1:p.Leu727=
NM_001278344.1:c.1555C= NP_001265273.1:p.Leu519=
NM_001278343.2:c.2179C= NP_001265272.1:p.Leu727=
NM_001103.4:c.2179C= MANE Select NP_001094.1:p.Leu727=
NM_001278344.2:c.1555C= NP_001265273.1:p.Leu519=