Canonical Allele Identifier: CA366702110

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568031G>A (hg19) ; chr7:g.5528400G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528400G>A , CM000669.2:g.5528400G>A	GRCh38
NC_000007.13:g.5568031G>A , CM000669.1:g.5568031G>A	GRCh37
NC_000007.12:g.5534557G>A	NCBI36
NG_007992.1:g.7202C>T , LRG_132:g.7202C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.683C>T	ENSP00000407473.2:p.Ala228Val
ENST00000473257.3:c.554C>T	ENSP00000501773.1:p.Ala185Val
ENST00000477812.2:n.1230C>T
ENST00000493945.6:c.683C>T	ENSP00000494269.1:p.Ala228Val
ENST00000642480.2:c.683C>T	ENSP00000495995.2:p.Ala228Val
ENST00000645576.1:c.635C>T	ENSP00000496101.1:p.Ala212Val
ENST00000646664.1:c.683C>T MANE Select	ENSP00000494750.1:p.Ala228Val
ENST00000647275.1:c.317C>T	ENSP00000494185.1:p.Ala106Val
ENST00000674681.1:c.683C>T	ENSP00000502821.1:p.Ala228Val
ENST00000675515.1:c.683C>T	ENSP00000501862.1:p.Ala228Val
ENST00000676189.1:c.*226C>T	ENSP00000502538.1:n.*226C>T
ENST00000676319.1:c.88-617C>T	ENSP00000502193.1:n.88-617C>T
ENST00000676397.1:c.683C>T	ENSP00000502286.1:p.Ala228Val
ENST00000331789.9:c.683C>T	ENSP00000349960.4:p.Ala228Val
ENST00000425660.5:c.*346C>T	ENSP00000409264.1:n.*346C>T
ENST00000462494.5:n.1208C>T
ENST00000473257.1:n.401C>T
ENST00000484841.5:n.838C>T
ENST00000493945.5:n.689C>T
NM_001101.3:c.683C>T , LRG_132t1:c.683C>T	NP_001092.1:p.Ala228Val
XM_006715764.1:c.317C>T	XP_006715827.1:p.Ala106Val
NM_001101.4:c.683C>T	NP_001092.1:p.Ala228Val
NM_001101.5:c.683C>T MANE Select	NP_001092.1:p.Ala228Val