Canonical Allele Identifier: CA1684977222
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529375T= , CM000669.2:g.5529375T= GRCh38
NC_000007.13:g.5569006T= , CM000669.1:g.5569006T= GRCh37
NC_000007.12:g.5535532T= NCBI36
NG_007992.1:g.6227A= , LRG_132:g.6227A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.149A= ENSP00000399487.2:p.Lys50=
ENST00000432588.6:c.149A= ENSP00000407473.2:p.Lys50=
ENST00000473257.3:c.20A= ENSP00000501773.1:p.Lys7=
ENST00000477812.2:n.356A=
ENST00000484841.6:n.303A=
ENST00000493945.6:c.149A= ENSP00000494269.1:p.Lys50=
ENST00000642480.2:c.149A= ENSP00000495995.2:p.Lys50=
ENST00000645025.1:n.232A=
ENST00000645576.1:c.149A= ENSP00000496101.1:p.Lys50=
ENST00000646664.1:c.149A= MANE Select ENSP00000494750.1:p.Lys50=
ENST00000647275.1:c.-3-656A= ENSP00000494185.1:n.-3-656A=
ENST00000674681.1:c.149A= ENSP00000502821.1:p.Lys50=
ENST00000675515.1:c.149A= ENSP00000501862.1:p.Lys50=
ENST00000676189.1:c.149A= ENSP00000502538.1:p.Lys50=
ENST00000676319.1:c.87+196A= ENSP00000502193.1:n.87+196A=
ENST00000676397.1:c.149A= ENSP00000502286.1:p.Lys50=
ENST00000331789.9:c.149A= ENSP00000349960.4:p.Lys50=
ENST00000414620.1:c.149A= ENSP00000401032.1:p.Lys50=
ENST00000417101.1:c.158A= ENSP00000399487.1:p.Lys53=
ENST00000425660.5:c.149A= ENSP00000409264.1:p.Lys50=
ENST00000432588.5:c.149A= ENSP00000407473.1:p.Lys50=
ENST00000443528.5:c.149A= ENSP00000393951.1:p.Lys50=
ENST00000462494.5:n.233A=
ENST00000473257.1:n.82-656A=
ENST00000477812.1:n.356A=
ENST00000480301.1:n.349A=
ENST00000484841.5:n.304A=
ENST00000493945.5:n.155A=
NM_001101.3:c.149A= , LRG_132t1:c.149A= NP_001092.1:p.Lys50=
NM_001101.4:c.149A= NP_001092.1:p.Lys50=
NM_001101.5:c.149A= MANE Select NP_001092.1:p.Lys50=