Canonical Allele Identifier: CA2697553811

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527994A>T , CM000669.2:g.5527994A>T	GRCh38
NC_000007.13:g.5567625A>T , CM000669.1:g.5567625A>T	GRCh37
NC_000007.12:g.5534151A>T	NCBI36
NG_007992.1:g.7608T>A , LRG_132:g.7608T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001101.5:c.984+10T>A MANE Select	NP_001092.1:n.984+10T>A
ENST00000646664.1:c.984+10T>A MANE Select	ENSP00000494750.1:n.984+10T>A
NM_001101.3:c.984+10T>A , LRG_132t1:c.984+10T>A	NP_001092.1:n.984+10T>A
NM_001101.4:c.984+10T>A	NP_001092.1:n.984+10T>A
ENST00000331789.9:c.984+10T>A	ENSP00000349960.4:n.984+10T>A
ENST00000425660.5:c.*647+10T>A	ENSP00000409264.1:n.*647+10T>A
ENST00000432588.6:c.994T>A	ENSP00000407473.2:p.Phe332Ile
ENST00000462494.5:n.1509+10T>A
ENST00000464611.1:n.95+10T>A
ENST00000473257.3:c.855+10T>A	ENSP00000501773.1:n.855+10T>A
ENST00000477812.2:n.1531+10T>A
ENST00000493945.5:n.1085+10T>A
ENST00000493945.6:c.984+10T>A	ENSP00000494269.1:n.984+10T>A
ENST00000642480.2:c.984+10T>A	ENSP00000495995.2:n.984+10T>A
ENST00000674681.1:c.984+10T>A	ENSP00000502821.1:n.984+10T>A
ENST00000675515.1:c.984+10T>A	ENSP00000501862.1:n.984+10T>A
ENST00000676189.1:c.*527+10T>A	ENSP00000502538.1:n.*527+10T>A
ENST00000676319.1:c.88-211T>A	ENSP00000502193.1:n.88-211T>A
ENST00000676397.1:c.994T>A	ENSP00000502286.1:p.Phe332Ile
XM_006715764.1:c.618+10T>A	XP_006715827.1:n.618+10T>A