Canonical Allele Identifier: CA2681649855

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528949-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528950dup , CM000669.2:g.5528950dup	GRCh38
NC_000007.13:g.5568581dup , CM000669.1:g.5568581dup	GRCh37
NC_000007.12:g.5535107dup	NCBI36
NG_007992.1:g.6652dup , LRG_132:g.6652dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+211dup	ENSP00000407473.2:n.363+211dup
ENST00000473257.3:c.234+211dup	ENSP00000501773.1:n.234+211dup
ENST00000477812.2:n.680dup
ENST00000484841.6:n.558+69dup
ENST00000493945.6:c.363+211dup	ENSP00000494269.1:n.363+211dup
ENST00000642480.2:c.363+211dup	ENSP00000495995.2:n.363+211dup
ENST00000645025.1:n.556dup
ENST00000645576.1:c.363+211dup	ENSP00000496101.1:n.363+211dup
ENST00000646664.1:c.363+211dup MANE Select	ENSP00000494750.1:n.363+211dup
ENST00000647275.1:c.-3-231dup	ENSP00000494185.1:n.-3-231dup
ENST00000674681.1:c.363+211dup	ENSP00000502821.1:n.363+211dup
ENST00000675515.1:c.363+211dup	ENSP00000501862.1:n.363+211dup
ENST00000676189.1:c.374+200dup	ENSP00000502538.1:n.374+200dup
ENST00000676319.1:c.87+621dup	ENSP00000502193.1:n.87+621dup
ENST00000676397.1:c.363+211dup	ENSP00000502286.1:n.363+211dup
ENST00000331789.9:c.363+211dup	ENSP00000349960.4:n.363+211dup
ENST00000425660.5:c.*26+69dup	ENSP00000409264.1:n.*26+69dup
ENST00000432588.5:c.363+211dup	ENSP00000407473.1:n.363+211dup
ENST00000462494.5:n.658dup
ENST00000473257.1:n.82-231dup
ENST00000477812.1:n.570+211dup
ENST00000484841.5:n.518+211dup
ENST00000493945.5:n.369+211dup
NM_001101.3:c.363+211dup , LRG_132t1:c.363+211dup	NP_001092.1:n.363+211dup
XM_006715764.1:c.-234dup	XP_006715827.1:n.-234dup
NM_001101.4:c.363+211dup	NP_001092.1:n.363+211dup
NM_001101.5:c.363+211dup MANE Select	NP_001092.1:n.363+211dup