Canonical Allele Identifier: CA1684977584
Gene: ACTB HGNC NCBI

Linked Data

dbSNP Id: rs1784838343

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529530_5529531dup , CM000669.2:g.5529530_5529531dup GRCh38
NC_000007.13:g.5569161_5569162dup , CM000669.1:g.5569161_5569162dup GRCh37
NC_000007.12:g.5535687_5535688dup NCBI36
NG_007992.1:g.6073_6074dup , LRG_132:g.6073_6074dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.123+6_123+7dup ENSP00000399487.2:n.123+6_123+7dup
ENST00000432588.6:c.123+6_123+7dup ENSP00000407473.2:n.123+6_123+7dup
ENST00000473257.3:c.-6-129_-6-128dup ENSP00000501773.1:n.-6-129_-6-128dup
ENST00000477812.2:n.202_203dup
ENST00000484841.6:n.277+6_277+7dup
ENST00000493945.6:c.123+6_123+7dup ENSP00000494269.1:n.123+6_123+7dup
ENST00000642480.2:c.123+6_123+7dup ENSP00000495995.2:n.123+6_123+7dup
ENST00000645025.1:n.206+6_206+7dup
ENST00000645576.1:c.123+6_123+7dup ENSP00000496101.1:n.123+6_123+7dup
ENST00000646664.1:c.123+6_123+7dup MANE Select ENSP00000494750.1:n.123+6_123+7dup
ENST00000647275.1:c.-3-810_-3-809dup ENSP00000494185.1:n.-3-810_-3-809dup
ENST00000674681.1:c.123+6_123+7dup ENSP00000502821.1:n.123+6_123+7dup
ENST00000675515.1:c.123+6_123+7dup ENSP00000501862.1:n.123+6_123+7dup
ENST00000676189.1:c.123+6_123+7dup ENSP00000502538.1:n.123+6_123+7dup
ENST00000676319.1:c.87+42_87+43dup ENSP00000502193.1:n.87+42_87+43dup
ENST00000676397.1:c.123+6_123+7dup ENSP00000502286.1:n.123+6_123+7dup
ENST00000331789.9:c.123+6_123+7dup ENSP00000349960.4:n.123+6_123+7dup
ENST00000414620.1:c.123+6_123+7dup ENSP00000401032.1:n.123+6_123+7dup
ENST00000417101.1:c.132+6_132+7dup ENSP00000399487.1:n.132+6_132+7dup
ENST00000425660.5:c.123+6_123+7dup ENSP00000409264.1:n.123+6_123+7dup
ENST00000432588.5:c.123+6_123+7dup ENSP00000407473.1:n.123+6_123+7dup
ENST00000443528.5:c.123+6_123+7dup ENSP00000393951.1:n.123+6_123+7dup
ENST00000462494.5:n.207+6_207+7dup
ENST00000473257.1:n.82-810_82-809dup
ENST00000477812.1:n.202_203dup
ENST00000480301.1:n.195_196dup
ENST00000484841.5:n.278+6_278+7dup
ENST00000493945.5:n.129+6_129+7dup
NM_001101.3:c.123+6_123+7dup , LRG_132t1:c.123+6_123+7dup NP_001092.1:n.123+6_123+7dup
NM_001101.4:c.123+6_123+7dup NP_001092.1:n.123+6_123+7dup
NM_001101.5:c.123+6_123+7dup MANE Select NP_001092.1:n.123+6_123+7dup