Canonical Allele Identifier: CA2487053184
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762467A= , CM000663.2:g.236762467A= GRCh38
NC_000001.10:g.236925767A= , CM000663.1:g.236925767A= GRCh37
NC_000001.9:g.234992390A= NCBI36
NG_009081.1:g.80998A=
NG_009081.2:g.103327A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2533A= ENSP00000443495.1:p.Ile845=
ENST00000461367.2:n.829A=
ENST00000492634.7:n.2463A=
ENST00000682015.1:c.2440A= ENSP00000506961.1:p.Ile814=
ENST00000682490.1:n.451A=
ENST00000682692.1:n.3628A=
ENST00000682966.1:n.8174A=
ENST00000683111.1:c.*1819A= ENSP00000507913.1:n.*1819A=
ENST00000683322.1:n.3885A=
ENST00000683805.1:n.1324A=
ENST00000684050.1:n.5171A=
ENST00000684122.1:n.1967A=
ENST00000684286.1:n.4088A=
ENST00000684502.1:n.3830A=
ENST00000684763.1:n.1148A=
ENST00000366578.6:c.2533A= MANE Select ENSP00000355537.4:p.Ile845=
ENST00000492634.6:n.2463A=
ENST00000542672.6:c.2533A= ENSP00000443495.1:p.Ile845=
ENST00000651091.1:c.2223A= ENSP00000498677.1:n.2223A=
ENST00000651275.1:c.2425A= ENSP00000498926.1:p.Ile809=
ENST00000651781.1:c.1613A=
ENST00000651786.1:c.*1905A= ENSP00000498364.1:n.*1905A=
ENST00000652096.1:c.*1938A= ENSP00000498896.1:n.*1938A=
ENST00000366578.5:c.2533A= ENSP00000355537.4:p.Ile845=
ENST00000461367.1:n.742A=
ENST00000542672.5:c.2533A= ENSP00000443495.1:p.Ile845=
ENST00000546208.5:c.1909A= ENSP00000438384.2:p.Ile637=
NM_001103.3:c.2533A= NP_001094.1:p.Ile845=
NM_001278343.1:c.2533A= NP_001265272.1:p.Ile845=
NM_001278344.1:c.1909A= NP_001265273.1:p.Ile637=
NM_001278343.2:c.2533A= NP_001265272.1:p.Ile845=
NM_001103.4:c.2533A= MANE Select NP_001094.1:p.Ile845=
NM_001278344.2:c.1909A= NP_001265273.1:p.Ile637=