Canonical Allele Identifier: CA345392089
Gene: ACTN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762476G>A , CM000663.2:g.236762476G>A GRCh38
NC_000001.10:g.236925776G>A , CM000663.1:g.236925776G>A GRCh37
NC_000001.9:g.234992399G>A NCBI36
NG_009081.1:g.81007G>A
NG_009081.2:g.103336G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2542G>A ENSP00000443495.1:p.Glu848Lys
ENST00000461367.2:n.838G>A
ENST00000492634.7:n.2472G>A
ENST00000682015.1:c.2449G>A ENSP00000506961.1:p.Glu817Lys
ENST00000682490.1:n.460G>A
ENST00000682692.1:n.3637G>A
ENST00000682966.1:n.8183G>A
ENST00000683111.1:c.*1828G>A ENSP00000507913.1:n.*1828G>A
ENST00000683322.1:n.3894G>A
ENST00000683805.1:n.1333G>A
ENST00000684050.1:n.5180G>A
ENST00000684122.1:n.1976G>A
ENST00000684286.1:n.4097G>A
ENST00000684502.1:n.3839G>A
ENST00000684763.1:n.1157G>A
ENST00000366578.6:c.2542G>A MANE Select ENSP00000355537.4:p.Glu848Lys
ENST00000492634.6:n.2472G>A
ENST00000542672.6:c.2542G>A ENSP00000443495.1:p.Glu848Lys
ENST00000651091.1:c.2232G>A ENSP00000498677.1:n.2232G>A
ENST00000651275.1:c.2434G>A ENSP00000498926.1:p.Glu812Lys
ENST00000651781.1:c.1622G>A
ENST00000651786.1:c.*1914G>A ENSP00000498364.1:n.*1914G>A
ENST00000652096.1:c.*1947G>A ENSP00000498896.1:n.*1947G>A
ENST00000366578.5:c.2542G>A ENSP00000355537.4:p.Glu848Lys
ENST00000461367.1:n.751G>A
ENST00000542672.5:c.2542G>A ENSP00000443495.1:p.Glu848Lys
ENST00000546208.5:c.1918G>A ENSP00000438384.2:p.Glu640Lys
NM_001103.3:c.2542G>A NP_001094.1:p.Glu848Lys
NM_001278343.1:c.2542G>A NP_001265272.1:p.Glu848Lys
NM_001278344.1:c.1918G>A NP_001265273.1:p.Glu640Lys
NM_001278343.2:c.2542G>A NP_001265272.1:p.Glu848Lys
NM_001103.4:c.2542G>A MANE Select NP_001094.1:p.Glu848Lys
NM_001278344.2:c.1918G>A NP_001265273.1:p.Glu640Lys