Canonical Allele Identifier: CA645558739

Gene: ACTB

Linked Data

• COSMIC: COSM6042072

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528723_5529163del , CM000669.2:g.5528723_5529163del	GRCh38
NC_000007.13:g.5568354_5568794del , CM000669.1:g.5568354_5568794del	GRCh37
NC_000007.12:g.5534880_5535320del	NCBI36
NG_007992.1:g.6442_6882del , LRG_132:g.6442_6882del

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.363+1_364-1del
ENST00000473257.3:c.234+1_235-1del
ENST00000477812.2:n.570+1_910del
ENST00000484841.6:n.517+1_559-1del
ENST00000493945.6:c.363+1_364-1del
ENST00000642480.2:c.363+1_364-1del
ENST00000645576.1:c.363+1_364-49del
ENST00000646664.1:c.363+1_364-1del
ENST00000647275.1:c.-3-441_-3-1del	ENSP00000494185.1:n.-3-441_-3-1del
ENST00000674681.1:c.363+1_364-1del
ENST00000675515.1:c.363+1_364-1del
ENST00000676189.1:c.364_375-13del
ENST00000676319.1:c.87+411_87+851del	ENSP00000502193.1:n.87+411_87+851del
ENST00000676397.1:c.363+1_364-1del
ENST00000331789.9:c.363+1_364-1del
ENST00000425660.5:c.363+1_*27-1del
ENST00000432588.5:c.363+1_364-1del
ENST00000462494.5:n.448_888del
ENST00000473257.1:n.82-441_82-1del
ENST00000477812.1:n.570+1_571-1del
ENST00000484841.5:n.518+1_519-1del
ENST00000493945.5:n.369+1_370-1del
NM_001101.3:c.363+1_364-1del , LRG_132t1:c.363+1_364-1del
XM_006715764.1:c.-344+1_-4del
NM_001101.4:c.363+1_364-1del
NM_001101.5:c.363+1_364-1del