Canonical Allele Identifier: CA453520248

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5527754G>A , CM000669.2:g.5527754G>A	GRCh38
NC_000007.13:g.5567385G>A , CM000669.1:g.5567385G>A	GRCh37
NC_000007.12:g.5533911G>A	NCBI36
NG_007992.1:g.7848C>T , LRG_132:g.7848C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473257.3:c.993C>T	ENSP00000501773.1:p.Cys331=
ENST00000477812.2:n.1669C>T
ENST00000493945.6:c.1122C>T	ENSP00000494269.1:p.Cys374=
ENST00000642480.2:c.1122C>T	ENSP00000495995.2:p.Cys374=
ENST00000646664.1:c.1122C>T MANE Select	ENSP00000494750.1:p.Cys374=
ENST00000674681.1:c.1122C>T	ENSP00000502821.1:p.Cys374=
ENST00000675515.1:c.1122C>T	ENSP00000501862.1:p.Cys374=
ENST00000676189.1:c.*665C>T	ENSP00000502538.1:n.*665C>T
ENST00000676319.1:c.117C>T	ENSP00000502193.1:p.Cys39=
ENST00000676397.1:c.*128C>T	ENSP00000502286.1:n.*128C>T
ENST00000331789.9:c.1122C>T	ENSP00000349960.4:p.Cys374=
ENST00000425660.5:c.*785C>T	ENSP00000409264.1:n.*785C>T
ENST00000462494.5:n.1647C>T
ENST00000464611.1:n.233C>T
ENST00000493945.5:n.1223C>T
NM_001101.3:c.1122C>T , LRG_132t1:c.1122C>T	NP_001092.1:p.Cys374=
XM_006715764.1:c.756C>T	XP_006715827.1:p.Cys252=
NM_001101.4:c.1122C>T	NP_001092.1:p.Cys374=
NM_001101.5:c.1122C>T MANE Select	NP_001092.1:p.Cys374=