Canonical Allele Identifier: CA2651182879
Gene: ACTN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762723_236762726dup , CM000663.2:g.236762723_236762726dup GRCh38
NC_000001.10:g.236926023_236926026dup , CM000663.1:g.236926023_236926026dup GRCh37
NC_000001.9:g.234992646_234992649dup NCBI36
NG_009081.1:g.81254_81257dup
NG_009081.2:g.103583_103586dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.*104_*107dup ENSP00000443495.1:n.*104_*107dup
ENST00000461367.2:n.1085_1088dup
ENST00000492634.7:n.2719_2722dup
ENST00000682015.1:c.*104_*107dup ENSP00000506961.1:n.*104_*107dup
ENST00000682490.1:n.707_710dup
ENST00000682692.1:n.3884_3887dup
ENST00000682966.1:n.8430_8433dup
ENST00000683111.1:c.*2075_*2078dup ENSP00000507913.1:n.*2075_*2078dup
ENST00000683322.1:n.4141_4144dup
ENST00000683805.1:n.1580_1583dup
ENST00000684050.1:n.5427_5430dup
ENST00000684122.1:n.2223_2226dup
ENST00000684286.1:n.4344_4347dup
ENST00000684502.1:n.4086_4089dup
ENST00000684763.1:n.1404_1407dup
ENST00000366578.6:c.*104_*107dup MANE Select ENSP00000355537.4:n.*104_*107dup
ENST00000492634.6:n.2719_2722dup
ENST00000542672.6:c.*104_*107dup ENSP00000443495.1:n.*104_*107dup
ENST00000651275.1:c.2681_2684dup ENSP00000498926.1:n.2681_2684dup
ENST00000651781.1:c.1869_1872dup
ENST00000652096.1:c.*2194_*2197dup ENSP00000498896.1:n.*2194_*2197dup
ENST00000366578.5:c.*104_*107dup ENSP00000355537.4:n.*104_*107dup
ENST00000542672.5:c.*104_*107dup ENSP00000443495.1:n.*104_*107dup
ENST00000546208.5:c.*104_*107dup ENSP00000438384.2:n.*104_*107dup
NM_001103.3:c.*104_*107dup NP_001094.1:n.*104_*107dup
NM_001278343.1:c.*104_*107dup NP_001265272.1:n.*104_*107dup
NM_001278344.1:c.*104_*107dup NP_001265273.1:n.*104_*107dup
NM_001278343.2:c.*104_*107dup NP_001265272.1:n.*104_*107dup
NM_001103.4:c.*104_*107dup MANE Select NP_001094.1:n.*104_*107dup
NM_001278344.2:c.*104_*107dup NP_001265273.1:n.*104_*107dup