Canonical Allele Identifier: CA4146889

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528004C>T , CM000669.2:g.5528004C>T	GRCh38
NC_000007.13:g.5567635C>T , CM000669.1:g.5567635C>T	GRCh37
NC_000007.12:g.5534161C>T	NCBI36
NG_007992.1:g.7598G>A , LRG_132:g.7598G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.984G>A	ENSP00000407473.2:p.Lys328=
ENST00000473257.3:c.855G>A	ENSP00000501773.1:p.Lys285=
ENST00000477812.2:n.1531G>A
ENST00000493945.6:c.984G>A	ENSP00000494269.1:p.Lys328=
ENST00000642480.2:c.984G>A	ENSP00000495995.2:p.Lys328=
ENST00000646664.1:c.984G>A MANE Select	ENSP00000494750.1:p.Lys328=
ENST00000674681.1:c.984G>A	ENSP00000502821.1:p.Lys328=
ENST00000675515.1:c.984G>A	ENSP00000501862.1:p.Lys328=
ENST00000676189.1:c.*527G>A	ENSP00000502538.1:n.*527G>A
ENST00000676319.1:c.88-221G>A	ENSP00000502193.1:n.88-221G>A
ENST00000676397.1:c.984G>A	ENSP00000502286.1:p.Lys328=
ENST00000331789.9:c.984G>A	ENSP00000349960.4:p.Lys328=
ENST00000425660.5:c.*647G>A	ENSP00000409264.1:n.*647G>A
ENST00000462494.5:n.1509G>A
ENST00000464611.1:n.95G>A
ENST00000493945.5:n.1085G>A
NM_001101.3:c.984G>A , LRG_132t1:c.984G>A	NP_001092.1:p.Lys328=
XM_006715764.1:c.618G>A	XP_006715827.1:p.Lys206=
NM_001101.4:c.984G>A	NP_001092.1:p.Lys328=
NM_001101.5:c.984G>A MANE Select	NP_001092.1:p.Lys328=