Canonical Allele Identifier: CA1684975842
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528609C= , CM000669.2:g.5528609C= GRCh38
NC_000007.13:g.5568240C= , CM000669.1:g.5568240C= GRCh37
NC_000007.12:g.5534766C= NCBI36
NG_007992.1:g.6993G= , LRG_132:g.6993G=

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.474G= ENSP00000407473.2:p.Gly158=
ENST00000473257.3:c.345G= ENSP00000501773.1:p.Gly115=
ENST00000477812.2:n.1021G=
ENST00000493945.6:c.474G= ENSP00000494269.1:p.Gly158=
ENST00000642480.2:c.474G= ENSP00000495995.2:p.Gly158=
ENST00000645576.1:c.426G= ENSP00000496101.1:p.Gly142=
ENST00000646664.1:c.474G= MANE Select ENSP00000494750.1:p.Gly158=
ENST00000647275.1:c.108G= ENSP00000494185.1:p.Gly36=
ENST00000674681.1:c.474G= ENSP00000502821.1:p.Gly158=
ENST00000675515.1:c.474G= ENSP00000501862.1:p.Gly158=
ENST00000676189.1:c.*17G= ENSP00000502538.1:n.*17G=
ENST00000676319.1:c.88-826G= ENSP00000502193.1:n.88-826G=
ENST00000676397.1:c.474G= ENSP00000502286.1:p.Gly158=
ENST00000331789.9:c.474G= ENSP00000349960.4:p.Gly158=
ENST00000425660.5:c.*137G= ENSP00000409264.1:n.*137G=
ENST00000432588.5:c.474G= ENSP00000407473.1:p.Gly158=
ENST00000462494.5:n.999G=
ENST00000473257.1:n.192G=
ENST00000477812.1:n.681G=
ENST00000484841.5:n.629G=
ENST00000493945.5:n.480G=
NM_001101.3:c.474G= , LRG_132t1:c.474G= NP_001092.1:p.Gly158=
XM_006715764.1:c.108G= XP_006715827.1:p.Gly36=
NM_001101.4:c.474G= NP_001092.1:p.Gly158=
NM_001101.5:c.474G= MANE Select NP_001092.1:p.Gly158=