Canonical Allele Identifier: CA2487050340
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236755102C= , CM000663.2:g.236755102C= GRCh38
NC_000001.10:g.236918402C= , CM000663.1:g.236918402C= GRCh37
NC_000001.9:g.234985025C= NCBI36
NG_009081.1:g.73633C=
NG_009081.2:g.95962C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542672.7:c.2058C= ENSP00000443495.1:p.Ile686=
ENST00000461367.2:n.354C=
ENST00000492634.7:n.1988C=
ENST00000682015.1:c.1965C= ENSP00000506961.1:p.Ile655=
ENST00000682692.1:n.3153C=
ENST00000682966.1:n.7699C=
ENST00000683111.1:c.*1344C= ENSP00000507913.1:n.*1344C=
ENST00000683322.1:n.3410C=
ENST00000683805.1:n.849C=
ENST00000684050.1:n.4696C=
ENST00000684122.1:n.205C=
ENST00000684286.1:n.3613C=
ENST00000684502.1:n.3355C=
ENST00000684763.1:n.673C=
ENST00000366578.6:c.2058C= MANE Select ENSP00000355537.4:p.Ile686=
ENST00000492634.6:n.1988C=
ENST00000542672.6:c.2058C= ENSP00000443495.1:p.Ile686=
ENST00000651091.1:c.1748C= ENSP00000498677.1:n.1748C=
ENST00000651275.1:c.1950C= ENSP00000498926.1:p.Ile650=
ENST00000651781.1:c.1138C=
ENST00000651786.1:c.*1430C= ENSP00000498364.1:n.*1430C=
ENST00000652096.1:c.*1463C= ENSP00000498896.1:n.*1463C=
ENST00000366578.5:c.2058C= ENSP00000355537.4:p.Ile686=
ENST00000461367.1:n.267C=
ENST00000542672.5:c.2058C= ENSP00000443495.1:p.Ile686=
ENST00000546208.5:c.1434C= ENSP00000438384.2:p.Ile478=
NM_001103.3:c.2058C= NP_001094.1:p.Ile686=
NM_001278343.1:c.2058C= NP_001265272.1:p.Ile686=
NM_001278344.1:c.1434C= NP_001265273.1:p.Ile478=
NM_001278343.2:c.2058C= NP_001265272.1:p.Ile686=
NM_001103.4:c.2058C= MANE Select NP_001094.1:p.Ile686=
NM_001278344.2:c.1434C= NP_001265273.1:p.Ile478=