Canonical Allele Identifier: CA1013665169
Gene: ACTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1659748419

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762723_236762725del , CM000663.2:g.236762723_236762725del GRCh38
NC_000001.10:g.236926023_236926025del , CM000663.1:g.236926023_236926025del GRCh37
NC_000001.9:g.234992646_234992648del NCBI36
NG_009081.1:g.81254_81256del
NG_009081.2:g.103583_103585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.*104_*106del ENSP00000443495.1:n.*104_*106del
ENST00000461367.2:n.1085_1087del
ENST00000492634.7:n.2719_2721del
ENST00000682015.1:c.*104_*106del ENSP00000506961.1:n.*104_*106del
ENST00000682490.1:n.707_709del
ENST00000682692.1:n.3884_3886del
ENST00000682966.1:n.8430_8432del
ENST00000683111.1:c.*2075_*2077del ENSP00000507913.1:n.*2075_*2077del
ENST00000683322.1:n.4141_4143del
ENST00000683805.1:n.1580_1582del
ENST00000684050.1:n.5427_5429del
ENST00000684122.1:n.2223_2225del
ENST00000684286.1:n.4344_4346del
ENST00000684502.1:n.4086_4088del
ENST00000684763.1:n.1404_1406del
ENST00000366578.6:c.*104_*106del MANE Select ENSP00000355537.4:n.*104_*106del
ENST00000492634.6:n.2719_2721del
ENST00000542672.6:c.*104_*106del ENSP00000443495.1:n.*104_*106del
ENST00000651275.1:c.2681_2683del ENSP00000498926.1:n.2681_2683del
ENST00000651781.1:c.1869_1871del
ENST00000652096.1:c.*2194_*2196del ENSP00000498896.1:n.*2194_*2196del
ENST00000366578.5:c.*104_*106del ENSP00000355537.4:n.*104_*106del
ENST00000542672.5:c.*104_*106del ENSP00000443495.1:n.*104_*106del
ENST00000546208.5:c.*104_*106del ENSP00000438384.2:n.*104_*106del
NM_001103.3:c.*104_*106del NP_001094.1:n.*104_*106del
NM_001278343.1:c.*104_*106del NP_001265272.1:n.*104_*106del
NM_001278344.1:c.*104_*106del NP_001265273.1:n.*104_*106del
NM_001278343.2:c.*104_*106del NP_001265272.1:n.*104_*106del
NM_001103.4:c.*104_*106del MANE Select NP_001094.1:n.*104_*106del
NM_001278344.2:c.*104_*106del NP_001265273.1:n.*104_*106del