Canonical Allele Identifier: CA366699064

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527795C>T , CM000669.2:g.5527795C>T	GRCh38
NC_000007.13:g.5567426C>T , CM000669.1:g.5567426C>T	GRCh37
NC_000007.12:g.5533952C>T	NCBI36
NG_007992.1:g.7807G>A , LRG_132:g.7807G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001101.5:c.1081G>A MANE Select	NP_001092.1:p.Glu361Lys
ENST00000646664.1:c.1081G>A MANE Select	ENSP00000494750.1:p.Glu361Lys
NM_001101.3:c.1081G>A , LRG_132t1:c.1081G>A	NP_001092.1:p.Glu361Lys
NM_001101.4:c.1081G>A	NP_001092.1:p.Glu361Lys
ENST00000331789.9:c.1081G>A	ENSP00000349960.4:p.Glu361Lys
ENST00000425660.5:c.*744G>A	ENSP00000409264.1:n.*744G>A
ENST00000462494.5:n.1606G>A
ENST00000464611.1:n.192G>A
ENST00000473257.3:c.952G>A	ENSP00000501773.1:p.Glu318Lys
ENST00000477812.2:n.1628G>A
ENST00000493945.5:n.1182G>A
ENST00000493945.6:c.1081G>A	ENSP00000494269.1:p.Glu361Lys
ENST00000642480.2:c.1081G>A	ENSP00000495995.2:p.Glu361Lys
ENST00000674681.1:c.1081G>A	ENSP00000502821.1:p.Glu361Lys
ENST00000675515.1:c.1081G>A	ENSP00000501862.1:p.Glu361Lys
ENST00000676189.1:c.*624G>A	ENSP00000502538.1:n.*624G>A
ENST00000676319.1:c.88-12G>A	ENSP00000502193.1:n.88-12G>A
ENST00000676397.1:c.*87G>A	ENSP00000502286.1:n.*87G>A
XM_006715764.1:c.715G>A	XP_006715827.1:p.Glu239Lys