Canonical Allele Identifier: CA2500220890
Gene: ACTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5528829_5528835del , CM000669.2:g.5528829_5528835del GRCh38
NC_000007.13:g.5568460_5568466del , CM000669.1:g.5568460_5568466del GRCh37
NC_000007.12:g.5534986_5534992del NCBI36
NG_007992.1:g.6767_6773del , LRG_132:g.6767_6773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432588.6:c.364-116_364-110del ENSP00000407473.2:n.364-116_364-110del
ENST00000473257.3:c.235-116_235-110del ENSP00000501773.1:n.235-116_235-110del
ENST00000477812.2:n.795_801del
ENST00000484841.6:n.559-116_559-110del
ENST00000493945.6:c.364-116_364-110del ENSP00000494269.1:n.364-116_364-110del
ENST00000642480.2:c.364-116_364-110del ENSP00000495995.2:n.364-116_364-110del
ENST00000645576.1:c.364-164_364-158del ENSP00000496101.1:n.364-164_364-158del
ENST00000646664.1:c.364-116_364-110del MANE Select ENSP00000494750.1:n.364-116_364-110del
ENST00000647275.1:c.-3-116_-3-110del ENSP00000494185.1:n.-3-116_-3-110del
ENST00000674681.1:c.364-116_364-110del ENSP00000502821.1:n.364-116_364-110del
ENST00000675515.1:c.364-116_364-110del ENSP00000501862.1:n.364-116_364-110del
ENST00000676189.1:c.375-128_375-122del ENSP00000502538.1:n.375-128_375-122del
ENST00000676319.1:c.87+736_87+742del ENSP00000502193.1:n.87+736_87+742del
ENST00000676397.1:c.364-116_364-110del ENSP00000502286.1:n.364-116_364-110del
ENST00000331789.9:c.364-116_364-110del ENSP00000349960.4:n.364-116_364-110del
ENST00000425660.5:c.*27-116_*27-110del ENSP00000409264.1:n.*27-116_*27-110del
ENST00000432588.5:c.364-116_364-110del ENSP00000407473.1:n.364-116_364-110del
ENST00000462494.5:n.773_779del
ENST00000473257.1:n.82-116_82-110del
ENST00000477812.1:n.571-116_571-110del
ENST00000484841.5:n.519-116_519-110del
ENST00000493945.5:n.370-116_370-110del
NM_001101.3:c.364-116_364-110del , LRG_132t1:c.364-116_364-110del NP_001092.1:n.364-116_364-110del
XM_006715764.1:c.-119_-113del XP_006715827.1:n.-119_-113del
NM_001101.4:c.364-116_364-110del NP_001092.1:n.364-116_364-110del
NM_001101.5:c.364-116_364-110del MANE Select NP_001092.1:n.364-116_364-110del