Canonical Allele Identifier: CA453639269

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528558-G-T
• MyVariant Identifiers: chr7:g.5568189G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528558G>T , CM000669.2:g.5528558G>T	GRCh38
NC_000007.13:g.5568189G>T , CM000669.1:g.5568189G>T	GRCh37
NC_000007.12:g.5534715G>T	NCBI36
NG_007992.1:g.7044C>A , LRG_132:g.7044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.525C>A	ENSP00000407473.2:p.Ile175=
ENST00000473257.3:c.396C>A	ENSP00000501773.1:p.Ile132=
ENST00000477812.2:n.1072C>A
ENST00000493945.6:c.525C>A	ENSP00000494269.1:p.Ile175=
ENST00000642480.2:c.525C>A	ENSP00000495995.2:p.Ile175=
ENST00000645576.1:c.477C>A	ENSP00000496101.1:p.Ile159=
ENST00000646664.1:c.525C>A MANE Select	ENSP00000494750.1:p.Ile175=
ENST00000647275.1:c.159C>A	ENSP00000494185.1:p.Ile53=
ENST00000674681.1:c.525C>A	ENSP00000502821.1:p.Ile175=
ENST00000675515.1:c.525C>A	ENSP00000501862.1:p.Ile175=
ENST00000676189.1:c.*68C>A	ENSP00000502538.1:n.*68C>A
ENST00000676319.1:c.88-775C>A	ENSP00000502193.1:n.88-775C>A
ENST00000676397.1:c.525C>A	ENSP00000502286.1:p.Ile175=
ENST00000331789.9:c.525C>A	ENSP00000349960.4:p.Ile175=
ENST00000425660.5:c.*188C>A	ENSP00000409264.1:n.*188C>A
ENST00000462494.5:n.1050C>A
ENST00000473257.1:n.243C>A
ENST00000477812.1:n.732C>A
ENST00000484841.5:n.680C>A
ENST00000493945.5:n.531C>A
NM_001101.3:c.525C>A , LRG_132t1:c.525C>A	NP_001092.1:p.Ile175=
XM_006715764.1:c.159C>A	XP_006715827.1:p.Ile53=
NM_001101.4:c.525C>A	NP_001092.1:p.Ile175=
NM_001101.5:c.525C>A MANE Select	NP_001092.1:p.Ile175=