Canonical Allele Identifier: CA366704995
Gene: ACTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529321T>G , CM000669.2:g.5529321T>G GRCh38
NC_000007.13:g.5568952T>G , CM000669.1:g.5568952T>G GRCh37
NC_000007.12:g.5535478T>G NCBI36
NG_007992.1:g.6281A>C , LRG_132:g.6281A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.203A>C ENSP00000399487.2:p.Lys68Thr
ENST00000432588.6:c.203A>C ENSP00000407473.2:p.Lys68Thr
ENST00000473257.3:c.74A>C ENSP00000501773.1:p.Lys25Thr
ENST00000477812.2:n.410A>C
ENST00000484841.6:n.357A>C
ENST00000493945.6:c.203A>C ENSP00000494269.1:p.Lys68Thr
ENST00000642480.2:c.203A>C ENSP00000495995.2:p.Lys68Thr
ENST00000645025.1:n.286A>C
ENST00000645576.1:c.203A>C ENSP00000496101.1:p.Lys68Thr
ENST00000646664.1:c.203A>C MANE Select ENSP00000494750.1:p.Lys68Thr
ENST00000647275.1:c.-3-602A>C ENSP00000494185.1:n.-3-602A>C
ENST00000674681.1:c.203A>C ENSP00000502821.1:p.Lys68Thr
ENST00000675515.1:c.203A>C ENSP00000501862.1:p.Lys68Thr
ENST00000676189.1:c.203A>C ENSP00000502538.1:p.Lys68Thr
ENST00000676319.1:c.87+250A>C ENSP00000502193.1:n.87+250A>C
ENST00000676397.1:c.203A>C ENSP00000502286.1:p.Lys68Thr
ENST00000331789.9:c.203A>C ENSP00000349960.4:p.Lys68Thr
ENST00000414620.1:c.203A>C ENSP00000401032.1:p.Lys68Thr
ENST00000417101.1:c.212A>C ENSP00000399487.1:p.Lys71Thr
ENST00000425660.5:c.203A>C ENSP00000409264.1:p.Lys68Thr
ENST00000432588.5:c.203A>C ENSP00000407473.1:p.Lys68Thr
ENST00000443528.5:c.203A>C ENSP00000393951.1:p.Lys68Thr
ENST00000462494.5:n.287A>C
ENST00000473257.1:n.82-602A>C
ENST00000477812.1:n.410A>C
ENST00000480301.1:n.403A>C
ENST00000484841.5:n.358A>C
ENST00000493945.5:n.209A>C
NM_001101.3:c.203A>C , LRG_132t1:c.203A>C NP_001092.1:p.Lys68Thr
NM_001101.4:c.203A>C NP_001092.1:p.Lys68Thr
NM_001101.5:c.203A>C MANE Select NP_001092.1:p.Lys68Thr