Canonical Allele Identifier: CA151574

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527853G>A , CM000669.2:g.5527853G>A	GRCh38
NC_000007.13:g.5567484G>A , CM000669.1:g.5567484G>A	GRCh37
NC_000007.12:g.5534010G>A	NCBI36
NG_007992.1:g.7749C>T , LRG_132:g.7749C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001101.5:c.1023C>T MANE Select	NP_001092.1:p.Ile341=
ENST00000646664.1:c.1023C>T MANE Select	ENSP00000494750.1:p.Ile341=
NM_001101.3:c.1023C>T , LRG_132t1:c.1023C>T	NP_001092.1:p.Ile341=
NM_001101.4:c.1023C>T	NP_001092.1:p.Ile341=
ENST00000331789.9:c.1023C>T	ENSP00000349960.4:p.Ile341=
ENST00000425660.5:c.*686C>T	ENSP00000409264.1:n.*686C>T
ENST00000432588.6:c.*130C>T	ENSP00000407473.2:n.*130C>T
ENST00000462494.5:n.1548C>T
ENST00000464611.1:n.134C>T
ENST00000473257.3:c.894C>T	ENSP00000501773.1:p.Ile298=
ENST00000477812.2:n.1570C>T
ENST00000493945.5:n.1124C>T
ENST00000493945.6:c.1023C>T	ENSP00000494269.1:p.Ile341=
ENST00000642480.2:c.1023C>T	ENSP00000495995.2:p.Ile341=
ENST00000674681.1:c.1023C>T	ENSP00000502821.1:p.Ile341=
ENST00000675515.1:c.1023C>T	ENSP00000501862.1:p.Ile341=
ENST00000676189.1:c.*566C>T	ENSP00000502538.1:n.*566C>T
ENST00000676319.1:c.88-70C>T	ENSP00000502193.1:n.88-70C>T
ENST00000676397.1:c.*29C>T	ENSP00000502286.1:n.*29C>T
XM_006715764.1:c.657C>T	XP_006715827.1:p.Ile219=