Canonical Allele Identifier: CA366698876

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527755C>T , CM000669.2:g.5527755C>T	GRCh38
NC_000007.13:g.5567386C>T , CM000669.1:g.5567386C>T	GRCh37
NC_000007.12:g.5533912C>T	NCBI36
NG_007992.1:g.7847G>A , LRG_132:g.7847G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001101.5:c.1121G>A MANE Select	NP_001092.1:p.Cys374Tyr
ENST00000646664.1:c.1121G>A MANE Select	ENSP00000494750.1:p.Cys374Tyr
NM_001101.3:c.1121G>A , LRG_132t1:c.1121G>A	NP_001092.1:p.Cys374Tyr
NM_001101.4:c.1121G>A	NP_001092.1:p.Cys374Tyr
ENST00000331789.9:c.1121G>A	ENSP00000349960.4:p.Cys374Tyr
ENST00000425660.5:c.*784G>A	ENSP00000409264.1:n.*784G>A
ENST00000462494.5:n.1646G>A
ENST00000464611.1:n.232G>A
ENST00000473257.3:c.992G>A	ENSP00000501773.1:p.Cys331Tyr
ENST00000477812.2:n.1668G>A
ENST00000493945.5:n.1222G>A
ENST00000493945.6:c.1121G>A	ENSP00000494269.1:p.Cys374Tyr
ENST00000642480.2:c.1121G>A	ENSP00000495995.2:p.Cys374Tyr
ENST00000674681.1:c.1121G>A	ENSP00000502821.1:p.Cys374Tyr
ENST00000675515.1:c.1121G>A	ENSP00000501862.1:p.Cys374Tyr
ENST00000676189.1:c.*664G>A	ENSP00000502538.1:n.*664G>A
ENST00000676319.1:c.116G>A	ENSP00000502193.1:p.Cys39Tyr
ENST00000676397.1:c.*127G>A	ENSP00000502286.1:n.*127G>A
XM_006715764.1:c.755G>A	XP_006715827.1:p.Cys252Tyr