Canonical Allele Identifier: CA2487053213
Gene: ACTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236762550A= , CM000663.2:g.236762550A= GRCh38
NC_000001.10:g.236925850A= , CM000663.1:g.236925850A= GRCh37
NC_000001.9:g.234992473A= NCBI36
NG_009081.1:g.81081A=
NG_009081.2:g.103410A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.2616A= ENSP00000443495.1:p.Pro872=
ENST00000461367.2:n.912A=
ENST00000492634.7:n.2546A=
ENST00000682015.1:c.2523A= ENSP00000506961.1:p.Pro841=
ENST00000682490.1:n.534A=
ENST00000682692.1:n.3711A=
ENST00000682966.1:n.8257A=
ENST00000683111.1:c.*1902A= ENSP00000507913.1:n.*1902A=
ENST00000683322.1:n.3968A=
ENST00000683805.1:n.1407A=
ENST00000684050.1:n.5254A=
ENST00000684122.1:n.2050A=
ENST00000684286.1:n.4171A=
ENST00000684502.1:n.3913A=
ENST00000684763.1:n.1231A=
ENST00000366578.6:c.2616A= MANE Select ENSP00000355537.4:p.Pro872=
ENST00000492634.6:n.2546A=
ENST00000542672.6:c.2616A= ENSP00000443495.1:p.Pro872=
ENST00000651091.1:c.2306A= ENSP00000498677.1:n.2306A=
ENST00000651275.1:c.2508A= ENSP00000498926.1:p.Pro836=
ENST00000651781.1:c.1696A=
ENST00000651786.1:c.*1988A= ENSP00000498364.1:n.*1988A=
ENST00000652096.1:c.*2021A= ENSP00000498896.1:n.*2021A=
ENST00000366578.5:c.2616A= ENSP00000355537.4:p.Pro872=
ENST00000461367.1:n.825A=
ENST00000542672.5:c.2616A= ENSP00000443495.1:p.Pro872=
ENST00000546208.5:c.1992A= ENSP00000438384.2:p.Pro664=
NM_001103.3:c.2616A= NP_001094.1:p.Pro872=
NM_001278343.1:c.2616A= NP_001265272.1:p.Pro872=
NM_001278344.1:c.1992A= NP_001265273.1:p.Pro664=
NM_001278343.2:c.2616A= NP_001265272.1:p.Pro872=
NM_001103.4:c.2616A= MANE Select NP_001094.1:p.Pro872=
NM_001278344.2:c.1992A= NP_001265273.1:p.Pro664=