Canonical Allele Identifier: CA345373450
Gene: ACTN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236718896G>T , CM000663.2:g.236718896G>T GRCh38
NC_000001.10:g.236882196G>T , CM000663.1:g.236882196G>T GRCh37
NC_000001.9:g.234948819G>T NCBI36
NG_009081.1:g.37427G>T
NG_009081.2:g.59756G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542672.7:c.244G>T ENSP00000443495.1:p.Glu82Ter
ENST00000492634.7:n.339G>T
ENST00000682015.1:c.244G>T ENSP00000506961.1:p.Glu82Ter
ENST00000682692.1:n.244G>T
ENST00000682966.1:n.243G>T
ENST00000683075.1:n.183G>T
ENST00000683111.1:c.187G>T ENSP00000507913.1:p.Glu63Ter
ENST00000684050.1:n.279G>T
ENST00000684286.1:n.312G>T
ENST00000684502.1:n.279G>T
ENST00000366578.6:c.244G>T MANE Select ENSP00000355537.4:p.Glu82Ter
ENST00000492634.6:n.339G>T
ENST00000542672.6:c.244G>T ENSP00000443495.1:p.Glu82Ter
ENST00000651091.1:c.187G>T ENSP00000498677.1:p.Glu63Ter
ENST00000651187.1:c.28G>T ENSP00000498348.1:p.Glu10Ter
ENST00000651275.1:c.229G>T ENSP00000498926.1:p.Glu77Ter
ENST00000651786.1:c.244G>T ENSP00000498364.1:p.Glu82Ter
ENST00000652096.1:c.244G>T ENSP00000498896.1:p.Glu82Ter
ENST00000366578.5:c.244G>T ENSP00000355537.4:p.Glu82Ter
ENST00000492634.5:n.391G>T
ENST00000542672.5:c.244G>T ENSP00000443495.1:p.Glu82Ter
ENST00000546208.5:c.-578G>T ENSP00000438384.2:n.-578G>T
NM_001103.3:c.244G>T NP_001094.1:p.Glu82Ter
NM_001278343.1:c.244G>T NP_001265272.1:p.Glu82Ter
NM_001278344.1:c.-578G>T NP_001265273.1:n.-578G>T
NM_001278343.2:c.244G>T NP_001265272.1:p.Glu82Ter
NM_001103.4:c.244G>T MANE Select NP_001094.1:p.Glu82Ter
NM_001278344.2:c.-578G>T NP_001265273.1:n.-578G>T