Canonical Allele Identifier: CA1684976490
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529000G= , CM000669.2:g.5529000G= GRCh38
NC_000007.13:g.5568631G= , CM000669.1:g.5568631G= GRCh37
NC_000007.12:g.5535157G= NCBI36
NG_007992.1:g.6602C= , LRG_132:g.6602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.363+161C= ENSP00000407473.2:n.363+161C=
ENST00000473257.3:c.234+161C= ENSP00000501773.1:n.234+161C=
ENST00000477812.2:n.630C=
ENST00000484841.6:n.558+19C=
ENST00000493945.6:c.363+161C= ENSP00000494269.1:n.363+161C=
ENST00000642480.2:c.363+161C= ENSP00000495995.2:n.363+161C=
ENST00000645025.1:n.506C=
ENST00000645576.1:c.363+161C= ENSP00000496101.1:n.363+161C=
ENST00000646664.1:c.363+161C= MANE Select ENSP00000494750.1:n.363+161C=
ENST00000647275.1:c.-3-281C= ENSP00000494185.1:n.-3-281C=
ENST00000674681.1:c.363+161C= ENSP00000502821.1:n.363+161C=
ENST00000675515.1:c.363+161C= ENSP00000501862.1:n.363+161C=
ENST00000676189.1:c.374+150C= ENSP00000502538.1:n.374+150C=
ENST00000676319.1:c.87+571C= ENSP00000502193.1:n.87+571C=
ENST00000676397.1:c.363+161C= ENSP00000502286.1:n.363+161C=
ENST00000331789.9:c.363+161C= ENSP00000349960.4:n.363+161C=
ENST00000425660.5:c.*26+19C= ENSP00000409264.1:n.*26+19C=
ENST00000432588.5:c.363+161C= ENSP00000407473.1:n.363+161C=
ENST00000462494.5:n.608C=
ENST00000473257.1:n.82-281C=
ENST00000477812.1:n.570+161C=
ENST00000484841.5:n.518+161C=
ENST00000493945.5:n.369+161C=
NM_001101.3:c.363+161C= , LRG_132t1:c.363+161C= NP_001092.1:n.363+161C=
XM_006715764.1:c.-284C= XP_006715827.1:n.-284C=
NM_001101.4:c.363+161C= NP_001092.1:n.363+161C=
NM_001101.5:c.363+161C= MANE Select NP_001092.1:n.363+161C=