Canonical Allele Identifier: CA366703552

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568253T>C (hg19) ; chr7:g.5528622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528622T>C , CM000669.2:g.5528622T>C	GRCh38
NC_000007.13:g.5568253T>C , CM000669.1:g.5568253T>C	GRCh37
NC_000007.12:g.5534779T>C	NCBI36
NG_007992.1:g.6980A>G , LRG_132:g.6980A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.461A>G	ENSP00000407473.2:p.Asp154Gly
ENST00000473257.3:c.332A>G	ENSP00000501773.1:p.Asp111Gly
ENST00000477812.2:n.1008A>G
ENST00000493945.6:c.461A>G	ENSP00000494269.1:p.Asp154Gly
ENST00000642480.2:c.461A>G	ENSP00000495995.2:p.Asp154Gly
ENST00000645576.1:c.413A>G	ENSP00000496101.1:p.Asp138Gly
ENST00000646664.1:c.461A>G MANE Select	ENSP00000494750.1:p.Asp154Gly
ENST00000647275.1:c.95A>G	ENSP00000494185.1:p.Asp32Gly
ENST00000674681.1:c.461A>G	ENSP00000502821.1:p.Asp154Gly
ENST00000675515.1:c.461A>G	ENSP00000501862.1:p.Asp154Gly
ENST00000676189.1:c.*4A>G	ENSP00000502538.1:n.*4A>G
ENST00000676319.1:c.88-839A>G	ENSP00000502193.1:n.88-839A>G
ENST00000676397.1:c.461A>G	ENSP00000502286.1:p.Asp154Gly
ENST00000331789.9:c.461A>G	ENSP00000349960.4:p.Asp154Gly
ENST00000425660.5:c.*124A>G	ENSP00000409264.1:n.*124A>G
ENST00000432588.5:c.461A>G	ENSP00000407473.1:p.Asp154Gly
ENST00000462494.5:n.986A>G
ENST00000473257.1:n.179A>G
ENST00000477812.1:n.668A>G
ENST00000484841.5:n.616A>G
ENST00000493945.5:n.467A>G
NM_001101.3:c.461A>G , LRG_132t1:c.461A>G	NP_001092.1:p.Asp154Gly
XM_006715764.1:c.95A>G	XP_006715827.1:p.Asp32Gly
NM_001101.4:c.461A>G	NP_001092.1:p.Asp154Gly
NM_001101.5:c.461A>G MANE Select	NP_001092.1:p.Asp154Gly