Canonical Allele Identifier: CA366704923
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529310C>A , CM000669.2:g.5529310C>A GRCh38
NC_000007.13:g.5568941C>A , CM000669.1:g.5568941C>A GRCh37
NC_000007.12:g.5535467C>A NCBI36
NG_007992.1:g.6292G>T , LRG_132:g.6292G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.214G>T ENSP00000399487.2:p.Glu72Ter
ENST00000432588.6:c.214G>T ENSP00000407473.2:p.Glu72Ter
ENST00000473257.3:c.85G>T ENSP00000501773.1:p.Glu29Ter
ENST00000477812.2:n.421G>T
ENST00000484841.6:n.368G>T
ENST00000493945.6:c.214G>T ENSP00000494269.1:p.Glu72Ter
ENST00000642480.2:c.214G>T ENSP00000495995.2:p.Glu72Ter
ENST00000645025.1:n.297G>T
ENST00000645576.1:c.214G>T ENSP00000496101.1:p.Glu72Ter
ENST00000646664.1:c.214G>T MANE Select ENSP00000494750.1:p.Glu72Ter
ENST00000647275.1:c.-3-591G>T ENSP00000494185.1:n.-3-591G>T
ENST00000674681.1:c.214G>T ENSP00000502821.1:p.Glu72Ter
ENST00000675515.1:c.214G>T ENSP00000501862.1:p.Glu72Ter
ENST00000676189.1:c.214G>T ENSP00000502538.1:p.Glu72Ter
ENST00000676319.1:c.87+261G>T ENSP00000502193.1:n.87+261G>T
ENST00000676397.1:c.214G>T ENSP00000502286.1:p.Glu72Ter
ENST00000331789.9:c.214G>T ENSP00000349960.4:p.Glu72Ter
ENST00000414620.1:c.214G>T ENSP00000401032.1:p.Glu72Ter
ENST00000417101.1:c.223G>T ENSP00000399487.1:p.Glu75Ter
ENST00000425660.5:c.214G>T ENSP00000409264.1:p.Glu72Ter
ENST00000432588.5:c.214G>T ENSP00000407473.1:p.Glu72Ter
ENST00000443528.5:c.214G>T ENSP00000393951.1:p.Glu72Ter
ENST00000462494.5:n.298G>T
ENST00000473257.1:n.82-591G>T
ENST00000477812.1:n.421G>T
ENST00000480301.1:n.414G>T
ENST00000484841.5:n.369G>T
ENST00000493945.5:n.220G>T
NM_001101.3:c.214G>T , LRG_132t1:c.214G>T NP_001092.1:p.Glu72Ter
NM_001101.4:c.214G>T NP_001092.1:p.Glu72Ter
NM_001101.5:c.214G>T MANE Select NP_001092.1:p.Glu72Ter