Canonical Allele Identifier: CA2487053195
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762504A= , CM000663.2:g.236762504A= GRCh38
NC_000001.10:g.236925804A= , CM000663.1:g.236925804A= GRCh37
NC_000001.9:g.234992427A= NCBI36
NG_009081.1:g.81035A=
NG_009081.2:g.103364A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2570A= ENSP00000443495.1:p.Asp857=
ENST00000461367.2:n.866A=
ENST00000492634.7:n.2500A=
ENST00000682015.1:c.2477A= ENSP00000506961.1:p.Asp826=
ENST00000682490.1:n.488A=
ENST00000682692.1:n.3665A=
ENST00000682966.1:n.8211A=
ENST00000683111.1:c.*1856A= ENSP00000507913.1:n.*1856A=
ENST00000683322.1:n.3922A=
ENST00000683805.1:n.1361A=
ENST00000684050.1:n.5208A=
ENST00000684122.1:n.2004A=
ENST00000684286.1:n.4125A=
ENST00000684502.1:n.3867A=
ENST00000684763.1:n.1185A=
ENST00000366578.6:c.2570A= MANE Select ENSP00000355537.4:p.Asp857=
ENST00000492634.6:n.2500A=
ENST00000542672.6:c.2570A= ENSP00000443495.1:p.Asp857=
ENST00000651091.1:c.2260A= ENSP00000498677.1:n.2260A=
ENST00000651275.1:c.2462A= ENSP00000498926.1:p.Asp821=
ENST00000651781.1:c.1650A=
ENST00000651786.1:c.*1942A= ENSP00000498364.1:n.*1942A=
ENST00000652096.1:c.*1975A= ENSP00000498896.1:n.*1975A=
ENST00000366578.5:c.2570A= ENSP00000355537.4:p.Asp857=
ENST00000461367.1:n.779A=
ENST00000542672.5:c.2570A= ENSP00000443495.1:p.Asp857=
ENST00000546208.5:c.1946A= ENSP00000438384.2:p.Asp649=
NM_001103.3:c.2570A= NP_001094.1:p.Asp857=
NM_001278343.1:c.2570A= NP_001265272.1:p.Asp857=
NM_001278344.1:c.1946A= NP_001265273.1:p.Asp649=
NM_001278343.2:c.2570A= NP_001265272.1:p.Asp857=
NM_001103.4:c.2570A= MANE Select NP_001094.1:p.Asp857=
NM_001278344.2:c.1946A= NP_001265273.1:p.Asp649=