Canonical Allele Identifier: CA453639238

Gene: ACTB

Linked Data

• gnomAD v3: 7-5528540-A-G
• gnomAD v4: 7-5528540-A-G
• MyVariant Identifiers: chr7:g.5568171A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528540A>G , CM000669.2:g.5528540A>G	GRCh38
NC_000007.13:g.5568171A>G , CM000669.1:g.5568171A>G	GRCh37
NC_000007.12:g.5534697A>G	NCBI36
NG_007992.1:g.7062T>C , LRG_132:g.7062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.543T>C	ENSP00000407473.2:p.Ala181=
ENST00000473257.3:c.414T>C	ENSP00000501773.1:p.Ala138=
ENST00000477812.2:n.1090T>C
ENST00000493945.6:c.543T>C	ENSP00000494269.1:p.Ala181=
ENST00000642480.2:c.543T>C	ENSP00000495995.2:p.Ala181=
ENST00000645576.1:c.495T>C	ENSP00000496101.1:p.Ala165=
ENST00000646664.1:c.543T>C MANE Select	ENSP00000494750.1:p.Ala181=
ENST00000647275.1:c.177T>C	ENSP00000494185.1:p.Ala59=
ENST00000674681.1:c.543T>C	ENSP00000502821.1:p.Ala181=
ENST00000675515.1:c.543T>C	ENSP00000501862.1:p.Ala181=
ENST00000676189.1:c.*86T>C	ENSP00000502538.1:n.*86T>C
ENST00000676319.1:c.88-757T>C	ENSP00000502193.1:n.88-757T>C
ENST00000676397.1:c.543T>C	ENSP00000502286.1:p.Ala181=
ENST00000331789.9:c.543T>C	ENSP00000349960.4:p.Ala181=
ENST00000425660.5:c.*206T>C	ENSP00000409264.1:n.*206T>C
ENST00000462494.5:n.1068T>C
ENST00000473257.1:n.261T>C
ENST00000477812.1:n.750T>C
ENST00000484841.5:n.698T>C
ENST00000493945.5:n.549T>C
NM_001101.3:c.543T>C , LRG_132t1:c.543T>C	NP_001092.1:p.Ala181=
XM_006715764.1:c.177T>C	XP_006715827.1:p.Ala59=
NM_001101.4:c.543T>C	NP_001092.1:p.Ala181=
NM_001101.5:c.543T>C MANE Select	NP_001092.1:p.Ala181=