Canonical Allele Identifier: CA4146833

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527769G>A , CM000669.2:g.5527769G>A	GRCh38
NC_000007.13:g.5567400G>A , CM000669.1:g.5567400G>A	GRCh37
NC_000007.12:g.5533926G>A	NCBI36
NG_007992.1:g.7833C>T , LRG_132:g.7833C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001101.5:c.1107C>T MANE Select	NP_001092.1:p.Ile369=
ENST00000646664.1:c.1107C>T MANE Select	ENSP00000494750.1:p.Ile369=
NM_001101.3:c.1107C>T , LRG_132t1:c.1107C>T	NP_001092.1:p.Ile369=
NM_001101.4:c.1107C>T	NP_001092.1:p.Ile369=
ENST00000331789.9:c.1107C>T	ENSP00000349960.4:p.Ile369=
ENST00000425660.5:c.*770C>T	ENSP00000409264.1:n.*770C>T
ENST00000462494.5:n.1632C>T
ENST00000464611.1:n.218C>T
ENST00000473257.3:c.978C>T	ENSP00000501773.1:p.Ile326=
ENST00000477812.2:n.1654C>T
ENST00000493945.5:n.1208C>T
ENST00000493945.6:c.1107C>T	ENSP00000494269.1:p.Ile369=
ENST00000642480.2:c.1107C>T	ENSP00000495995.2:p.Ile369=
ENST00000674681.1:c.1107C>T	ENSP00000502821.1:p.Ile369=
ENST00000675515.1:c.1107C>T	ENSP00000501862.1:p.Ile369=
ENST00000676189.1:c.*650C>T	ENSP00000502538.1:n.*650C>T
ENST00000676319.1:c.102C>T	ENSP00000502193.1:p.Ile34=
ENST00000676397.1:c.*113C>T	ENSP00000502286.1:n.*113C>T
XM_006715764.1:c.741C>T	XP_006715827.1:p.Ile247=