Canonical Allele Identifier: CA1684975925
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528723T= , CM000669.2:g.5528723T= GRCh38
NC_000007.13:g.5568354T= , CM000669.1:g.5568354T= GRCh37
NC_000007.12:g.5534880T= NCBI36
NG_007992.1:g.6879A= , LRG_132:g.6879A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-4A= ENSP00000407473.2:n.364-4A=
ENST00000473257.3:c.235-4A= ENSP00000501773.1:n.235-4A=
ENST00000477812.2:n.907A=
ENST00000484841.6:n.559-4A=
ENST00000493945.6:c.364-4A= ENSP00000494269.1:n.364-4A=
ENST00000642480.2:c.364-4A= ENSP00000495995.2:n.364-4A=
ENST00000645576.1:c.364-52A= ENSP00000496101.1:n.364-52A=
ENST00000646664.1:c.364-4A= MANE Select ENSP00000494750.1:n.364-4A=
ENST00000647275.1:c.-3-4A= ENSP00000494185.1:n.-3-4A=
ENST00000674681.1:c.364-4A= ENSP00000502821.1:n.364-4A=
ENST00000675515.1:c.364-4A= ENSP00000501862.1:n.364-4A=
ENST00000676189.1:c.375-16A= ENSP00000502538.1:n.375-16A=
ENST00000676319.1:c.87+848A= ENSP00000502193.1:n.87+848A=
ENST00000676397.1:c.364-4A= ENSP00000502286.1:n.364-4A=
ENST00000331789.9:c.364-4A= ENSP00000349960.4:n.364-4A=
ENST00000425660.5:c.*27-4A= ENSP00000409264.1:n.*27-4A=
ENST00000432588.5:c.364-4A= ENSP00000407473.1:n.364-4A=
ENST00000462494.5:n.885A=
ENST00000473257.1:n.82-4A=
ENST00000477812.1:n.571-4A=
ENST00000484841.5:n.519-4A=
ENST00000493945.5:n.370-4A=
NM_001101.3:c.364-4A= , LRG_132t1:c.364-4A= NP_001092.1:n.364-4A=
XM_006715764.1:c.-7A= XP_006715827.1:n.-7A=
NM_001101.4:c.364-4A= NP_001092.1:n.364-4A=
NM_001101.5:c.364-4A= MANE Select NP_001092.1:n.364-4A=