Canonical Allele Identifier: CA2681649850

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528940-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528940C>A , CM000669.2:g.5528940C>A	GRCh38
NC_000007.13:g.5568571C>A , CM000669.1:g.5568571C>A	GRCh37
NC_000007.12:g.5535097C>A	NCBI36
NG_007992.1:g.6662G>T , LRG_132:g.6662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-221G>T	ENSP00000407473.2:n.364-221G>T
ENST00000473257.3:c.235-221G>T	ENSP00000501773.1:n.235-221G>T
ENST00000477812.2:n.690G>T
ENST00000484841.6:n.558+79G>T
ENST00000493945.6:c.364-221G>T	ENSP00000494269.1:n.364-221G>T
ENST00000642480.2:c.364-221G>T	ENSP00000495995.2:n.364-221G>T
ENST00000645025.1:n.566G>T
ENST00000645576.1:c.363+221G>T	ENSP00000496101.1:n.363+221G>T
ENST00000646664.1:c.364-221G>T MANE Select	ENSP00000494750.1:n.364-221G>T
ENST00000647275.1:c.-3-221G>T	ENSP00000494185.1:n.-3-221G>T
ENST00000674681.1:c.364-221G>T	ENSP00000502821.1:n.364-221G>T
ENST00000675515.1:c.364-221G>T	ENSP00000501862.1:n.364-221G>T
ENST00000676189.1:c.374+210G>T	ENSP00000502538.1:n.374+210G>T
ENST00000676319.1:c.87+631G>T	ENSP00000502193.1:n.87+631G>T
ENST00000676397.1:c.364-221G>T	ENSP00000502286.1:n.364-221G>T
ENST00000331789.9:c.364-221G>T	ENSP00000349960.4:n.364-221G>T
ENST00000425660.5:c.*26+79G>T	ENSP00000409264.1:n.*26+79G>T
ENST00000432588.5:c.364-221G>T	ENSP00000407473.1:n.364-221G>T
ENST00000462494.5:n.668G>T
ENST00000473257.1:n.82-221G>T
ENST00000477812.1:n.571-221G>T
ENST00000484841.5:n.519-221G>T
ENST00000493945.5:n.370-221G>T
NM_001101.3:c.364-221G>T , LRG_132t1:c.364-221G>T	NP_001092.1:n.364-221G>T
XM_006715764.1:c.-224G>T	XP_006715827.1:n.-224G>T
NM_001101.4:c.364-221G>T	NP_001092.1:n.364-221G>T
NM_001101.5:c.364-221G>T MANE Select	NP_001092.1:n.364-221G>T