Canonical Allele Identifier: CA1684988373
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528514A= , CM000669.2:g.5528514A= GRCh38
NC_000007.13:g.5568145A= , CM000669.1:g.5568145A= GRCh37
NC_000007.12:g.5534671A= NCBI36
NG_007992.1:g.7088T= , LRG_132:g.7088T=

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.569T= ENSP00000407473.2:p.Met190=
ENST00000473257.3:c.440T= ENSP00000501773.1:p.Met147=
ENST00000477812.2:n.1116T=
ENST00000493945.6:c.569T= ENSP00000494269.1:p.Met190=
ENST00000642480.2:c.569T= ENSP00000495995.2:p.Met190=
ENST00000645576.1:c.521T= ENSP00000496101.1:p.Met174=
ENST00000646664.1:c.569T= MANE Select ENSP00000494750.1:p.Met190=
ENST00000647275.1:c.203T= ENSP00000494185.1:p.Met68=
ENST00000674681.1:c.569T= ENSP00000502821.1:p.Met190=
ENST00000675515.1:c.569T= ENSP00000501862.1:p.Met190=
ENST00000676189.1:c.*112T= ENSP00000502538.1:n.*112T=
ENST00000676319.1:c.88-731T= ENSP00000502193.1:n.88-731T=
ENST00000676397.1:c.569T= ENSP00000502286.1:p.Met190=
ENST00000331789.9:c.569T= ENSP00000349960.4:p.Met190=
ENST00000425660.5:c.*232T= ENSP00000409264.1:n.*232T=
ENST00000462494.5:n.1094T=
ENST00000473257.1:n.287T=
ENST00000477812.1:n.776T=
ENST00000484841.5:n.724T=
ENST00000493945.5:n.575T=
NM_001101.3:c.569T= , LRG_132t1:c.569T= NP_001092.1:p.Met190=
XM_006715764.1:c.203T= XP_006715827.1:p.Met68=
NM_001101.4:c.569T= NP_001092.1:p.Met190=
NM_001101.5:c.569T= MANE Select NP_001092.1:p.Met190=