Canonical Allele Identifier: CA1684988367
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528511T= , CM000669.2:g.5528511T= GRCh38
NC_000007.13:g.5568142T= , CM000669.1:g.5568142T= GRCh37
NC_000007.12:g.5534668T= NCBI36
NG_007992.1:g.7091A= , LRG_132:g.7091A=

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.572A= ENSP00000407473.2:p.Lys191=
ENST00000473257.3:c.443A= ENSP00000501773.1:p.Lys148=
ENST00000477812.2:n.1119A=
ENST00000493945.6:c.572A= ENSP00000494269.1:p.Lys191=
ENST00000642480.2:c.572A= ENSP00000495995.2:p.Lys191=
ENST00000645576.1:c.524A= ENSP00000496101.1:p.Lys175=
ENST00000646664.1:c.572A= MANE Select ENSP00000494750.1:p.Lys191=
ENST00000647275.1:c.206A= ENSP00000494185.1:p.Lys69=
ENST00000674681.1:c.572A= ENSP00000502821.1:p.Lys191=
ENST00000675515.1:c.572A= ENSP00000501862.1:p.Lys191=
ENST00000676189.1:c.*115A= ENSP00000502538.1:n.*115A=
ENST00000676319.1:c.88-728A= ENSP00000502193.1:n.88-728A=
ENST00000676397.1:c.572A= ENSP00000502286.1:p.Lys191=
ENST00000331789.9:c.572A= ENSP00000349960.4:p.Lys191=
ENST00000425660.5:c.*235A= ENSP00000409264.1:n.*235A=
ENST00000462494.5:n.1097A=
ENST00000473257.1:n.290A=
ENST00000477812.1:n.779A=
ENST00000484841.5:n.727A=
ENST00000493945.5:n.578A=
NM_001101.3:c.572A= , LRG_132t1:c.572A= NP_001092.1:p.Lys191=
XM_006715764.1:c.206A= XP_006715827.1:p.Lys69=
NM_001101.4:c.572A= NP_001092.1:p.Lys191=
NM_001101.5:c.572A= MANE Select NP_001092.1:p.Lys191=