Canonical Allele Identifier: CA2578822286

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528992-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528992G>A , CM000669.2:g.5528992G>A	GRCh38
NC_000007.13:g.5568623G>A , CM000669.1:g.5568623G>A	GRCh37
NC_000007.12:g.5535149G>A	NCBI36
NG_007992.1:g.6610C>T , LRG_132:g.6610C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+169C>T	ENSP00000407473.2:n.363+169C>T
ENST00000473257.3:c.234+169C>T	ENSP00000501773.1:n.234+169C>T
ENST00000477812.2:n.638C>T
ENST00000484841.6:n.558+27C>T
ENST00000493945.6:c.363+169C>T	ENSP00000494269.1:n.363+169C>T
ENST00000642480.2:c.363+169C>T	ENSP00000495995.2:n.363+169C>T
ENST00000645025.1:n.514C>T
ENST00000645576.1:c.363+169C>T	ENSP00000496101.1:n.363+169C>T
ENST00000646664.1:c.363+169C>T MANE Select	ENSP00000494750.1:n.363+169C>T
ENST00000647275.1:c.-3-273C>T	ENSP00000494185.1:n.-3-273C>T
ENST00000674681.1:c.363+169C>T	ENSP00000502821.1:n.363+169C>T
ENST00000675515.1:c.363+169C>T	ENSP00000501862.1:n.363+169C>T
ENST00000676189.1:c.374+158C>T	ENSP00000502538.1:n.374+158C>T
ENST00000676319.1:c.87+579C>T	ENSP00000502193.1:n.87+579C>T
ENST00000676397.1:c.363+169C>T	ENSP00000502286.1:n.363+169C>T
ENST00000331789.9:c.363+169C>T	ENSP00000349960.4:n.363+169C>T
ENST00000425660.5:c.*26+27C>T	ENSP00000409264.1:n.*26+27C>T
ENST00000432588.5:c.363+169C>T	ENSP00000407473.1:n.363+169C>T
ENST00000462494.5:n.616C>T
ENST00000473257.1:n.82-273C>T
ENST00000477812.1:n.570+169C>T
ENST00000484841.5:n.518+169C>T
ENST00000493945.5:n.369+169C>T
NM_001101.3:c.363+169C>T , LRG_132t1:c.363+169C>T	NP_001092.1:n.363+169C>T
XM_006715764.1:c.-276C>T	XP_006715827.1:n.-276C>T
NM_001101.4:c.363+169C>T	NP_001092.1:n.363+169C>T
NM_001101.5:c.363+169C>T MANE Select	NP_001092.1:n.363+169C>T