Canonical Allele Identifier: CA572821958
Gene: ACTB HGNC NCBI

Linked Data

dbSNP Id: rs1336813898

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529488_5529491dup , CM000669.2:g.5529488_5529491dup GRCh38
NC_000007.13:g.5569119_5569122dup , CM000669.1:g.5569119_5569122dup GRCh37
NC_000007.12:g.5535645_5535648dup NCBI36
NG_007992.1:g.6112_6115dup , LRG_132:g.6112_6115dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.123+45_123+48dup ENSP00000399487.2:n.123+45_123+48dup
ENST00000432588.6:c.123+45_123+48dup ENSP00000407473.2:n.123+45_123+48dup
ENST00000473257.3:c.-6-90_-6-87dup ENSP00000501773.1:n.-6-90_-6-87dup
ENST00000477812.2:n.241_244dup
ENST00000484841.6:n.277+45_277+48dup
ENST00000493945.6:c.123+45_123+48dup ENSP00000494269.1:n.123+45_123+48dup
ENST00000642480.2:c.123+45_123+48dup ENSP00000495995.2:n.123+45_123+48dup
ENST00000645025.1:n.206+45_206+48dup
ENST00000645576.1:c.123+45_123+48dup ENSP00000496101.1:n.123+45_123+48dup
ENST00000646664.1:c.123+45_123+48dup MANE Select ENSP00000494750.1:n.123+45_123+48dup
ENST00000647275.1:c.-3-771_-3-768dup ENSP00000494185.1:n.-3-771_-3-768dup
ENST00000674681.1:c.123+45_123+48dup ENSP00000502821.1:n.123+45_123+48dup
ENST00000675515.1:c.123+45_123+48dup ENSP00000501862.1:n.123+45_123+48dup
ENST00000676189.1:c.123+45_123+48dup ENSP00000502538.1:n.123+45_123+48dup
ENST00000676319.1:c.87+81_87+84dup ENSP00000502193.1:n.87+81_87+84dup
ENST00000676397.1:c.123+45_123+48dup ENSP00000502286.1:n.123+45_123+48dup
ENST00000331789.9:c.123+45_123+48dup ENSP00000349960.4:n.123+45_123+48dup
ENST00000414620.1:c.123+45_123+48dup ENSP00000401032.1:n.123+45_123+48dup
ENST00000417101.1:c.132+45_132+48dup ENSP00000399487.1:n.132+45_132+48dup
ENST00000425660.5:c.123+45_123+48dup ENSP00000409264.1:n.123+45_123+48dup
ENST00000432588.5:c.123+45_123+48dup ENSP00000407473.1:n.123+45_123+48dup
ENST00000443528.5:c.123+45_123+48dup ENSP00000393951.1:n.123+45_123+48dup
ENST00000462494.5:n.207+45_207+48dup
ENST00000473257.1:n.82-771_82-768dup
ENST00000477812.1:n.241_244dup
ENST00000480301.1:n.234_237dup
ENST00000484841.5:n.278+45_278+48dup
ENST00000493945.5:n.129+45_129+48dup
NM_001101.3:c.123+45_123+48dup , LRG_132t1:c.123+45_123+48dup NP_001092.1:n.123+45_123+48dup
NM_001101.4:c.123+45_123+48dup NP_001092.1:n.123+45_123+48dup
NM_001101.5:c.123+45_123+48dup MANE Select NP_001092.1:n.123+45_123+48dup