Canonical Allele Identifier: CA366703382

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568226A>G (hg19) ; chr7:g.5528595A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528595A>G , CM000669.2:g.5528595A>G	GRCh38
NC_000007.13:g.5568226A>G , CM000669.1:g.5568226A>G	GRCh37
NC_000007.12:g.5534752A>G	NCBI36
NG_007992.1:g.7007T>C , LRG_132:g.7007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.488T>C	ENSP00000407473.2:p.Val163Ala
ENST00000473257.3:c.359T>C	ENSP00000501773.1:p.Val120Ala
ENST00000477812.2:n.1035T>C
ENST00000493945.6:c.488T>C	ENSP00000494269.1:p.Val163Ala
ENST00000642480.2:c.488T>C	ENSP00000495995.2:p.Val163Ala
ENST00000645576.1:c.440T>C	ENSP00000496101.1:p.Val147Ala
ENST00000646664.1:c.488T>C MANE Select	ENSP00000494750.1:p.Val163Ala
ENST00000647275.1:c.122T>C	ENSP00000494185.1:p.Val41Ala
ENST00000674681.1:c.488T>C	ENSP00000502821.1:p.Val163Ala
ENST00000675515.1:c.488T>C	ENSP00000501862.1:p.Val163Ala
ENST00000676189.1:c.*31T>C	ENSP00000502538.1:n.*31T>C
ENST00000676319.1:c.88-812T>C	ENSP00000502193.1:n.88-812T>C
ENST00000676397.1:c.488T>C	ENSP00000502286.1:p.Val163Ala
ENST00000331789.9:c.488T>C	ENSP00000349960.4:p.Val163Ala
ENST00000425660.5:c.*151T>C	ENSP00000409264.1:n.*151T>C
ENST00000432588.5:c.488T>C	ENSP00000407473.1:p.Val163Ala
ENST00000462494.5:n.1013T>C
ENST00000473257.1:n.206T>C
ENST00000477812.1:n.695T>C
ENST00000484841.5:n.643T>C
ENST00000493945.5:n.494T>C
NM_001101.3:c.488T>C , LRG_132t1:c.488T>C	NP_001092.1:p.Val163Ala
XM_006715764.1:c.122T>C	XP_006715827.1:p.Val41Ala
NM_001101.4:c.488T>C	NP_001092.1:p.Val163Ala
NM_001101.5:c.488T>C MANE Select	NP_001092.1:p.Val163Ala