Canonical Allele Identifier: CA2681649858

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528953-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528955dup , CM000669.2:g.5528955dup	GRCh38
NC_000007.13:g.5568586dup , CM000669.1:g.5568586dup	GRCh37
NC_000007.12:g.5535112dup	NCBI36
NG_007992.1:g.6648dup , LRG_132:g.6648dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+207dup	ENSP00000407473.2:n.363+207dup
ENST00000473257.3:c.234+207dup	ENSP00000501773.1:n.234+207dup
ENST00000477812.2:n.676dup
ENST00000484841.6:n.558+65dup
ENST00000493945.6:c.363+207dup	ENSP00000494269.1:n.363+207dup
ENST00000642480.2:c.363+207dup	ENSP00000495995.2:n.363+207dup
ENST00000645025.1:n.552dup
ENST00000645576.1:c.363+207dup	ENSP00000496101.1:n.363+207dup
ENST00000646664.1:c.363+207dup MANE Select	ENSP00000494750.1:n.363+207dup
ENST00000647275.1:c.-3-235dup	ENSP00000494185.1:n.-3-235dup
ENST00000674681.1:c.363+207dup	ENSP00000502821.1:n.363+207dup
ENST00000675515.1:c.363+207dup	ENSP00000501862.1:n.363+207dup
ENST00000676189.1:c.374+196dup	ENSP00000502538.1:n.374+196dup
ENST00000676319.1:c.87+617dup	ENSP00000502193.1:n.87+617dup
ENST00000676397.1:c.363+207dup	ENSP00000502286.1:n.363+207dup
ENST00000331789.9:c.363+207dup	ENSP00000349960.4:n.363+207dup
ENST00000425660.5:c.*26+65dup	ENSP00000409264.1:n.*26+65dup
ENST00000432588.5:c.363+207dup	ENSP00000407473.1:n.363+207dup
ENST00000462494.5:n.654dup
ENST00000473257.1:n.82-235dup
ENST00000477812.1:n.570+207dup
ENST00000484841.5:n.518+207dup
ENST00000493945.5:n.369+207dup
NM_001101.3:c.363+207dup , LRG_132t1:c.363+207dup	NP_001092.1:n.363+207dup
XM_006715764.1:c.-238dup	XP_006715827.1:n.-238dup
NM_001101.4:c.363+207dup	NP_001092.1:n.363+207dup
NM_001101.5:c.363+207dup MANE Select	NP_001092.1:n.363+207dup