Canonical Allele Identifier: CA1684988380
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528516G= , CM000669.2:g.5528516G= GRCh38
NC_000007.13:g.5568147G= , CM000669.1:g.5568147G= GRCh37
NC_000007.12:g.5534673G= NCBI36
NG_007992.1:g.7086C= , LRG_132:g.7086C=

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.567C= ENSP00000407473.2:p.Leu189=
ENST00000473257.3:c.438C= ENSP00000501773.1:p.Leu146=
ENST00000477812.2:n.1114C=
ENST00000493945.6:c.567C= ENSP00000494269.1:p.Leu189=
ENST00000642480.2:c.567C= ENSP00000495995.2:p.Leu189=
ENST00000645576.1:c.519C= ENSP00000496101.1:p.Leu173=
ENST00000646664.1:c.567C= MANE Select ENSP00000494750.1:p.Leu189=
ENST00000647275.1:c.201C= ENSP00000494185.1:p.Leu67=
ENST00000674681.1:c.567C= ENSP00000502821.1:p.Leu189=
ENST00000675515.1:c.567C= ENSP00000501862.1:p.Leu189=
ENST00000676189.1:c.*110C= ENSP00000502538.1:n.*110C=
ENST00000676319.1:c.88-733C= ENSP00000502193.1:n.88-733C=
ENST00000676397.1:c.567C= ENSP00000502286.1:p.Leu189=
ENST00000331789.9:c.567C= ENSP00000349960.4:p.Leu189=
ENST00000425660.5:c.*230C= ENSP00000409264.1:n.*230C=
ENST00000462494.5:n.1092C=
ENST00000473257.1:n.285C=
ENST00000477812.1:n.774C=
ENST00000484841.5:n.722C=
ENST00000493945.5:n.573C=
NM_001101.3:c.567C= , LRG_132t1:c.567C= NP_001092.1:p.Leu189=
XM_006715764.1:c.201C= XP_006715827.1:p.Leu67=
NM_001101.4:c.567C= NP_001092.1:p.Leu189=
NM_001101.5:c.567C= MANE Select NP_001092.1:p.Leu189=