Canonical Allele Identifier: CA366703448

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568238A>T (hg19) ; chr7:g.5528607A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528607A>T , CM000669.2:g.5528607A>T	GRCh38
NC_000007.13:g.5568238A>T , CM000669.1:g.5568238A>T	GRCh37
NC_000007.12:g.5534764A>T	NCBI36
NG_007992.1:g.6995T>A , LRG_132:g.6995T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.476T>A	ENSP00000407473.2:p.Val159Asp
ENST00000473257.3:c.347T>A	ENSP00000501773.1:p.Val116Asp
ENST00000477812.2:n.1023T>A
ENST00000493945.6:c.476T>A	ENSP00000494269.1:p.Val159Asp
ENST00000642480.2:c.476T>A	ENSP00000495995.2:p.Val159Asp
ENST00000645576.1:c.428T>A	ENSP00000496101.1:p.Val143Asp
ENST00000646664.1:c.476T>A MANE Select	ENSP00000494750.1:p.Val159Asp
ENST00000647275.1:c.110T>A	ENSP00000494185.1:p.Val37Asp
ENST00000674681.1:c.476T>A	ENSP00000502821.1:p.Val159Asp
ENST00000675515.1:c.476T>A	ENSP00000501862.1:p.Val159Asp
ENST00000676189.1:c.*19T>A	ENSP00000502538.1:n.*19T>A
ENST00000676319.1:c.88-824T>A	ENSP00000502193.1:n.88-824T>A
ENST00000676397.1:c.476T>A	ENSP00000502286.1:p.Val159Asp
ENST00000331789.9:c.476T>A	ENSP00000349960.4:p.Val159Asp
ENST00000425660.5:c.*139T>A	ENSP00000409264.1:n.*139T>A
ENST00000432588.5:c.476T>A	ENSP00000407473.1:p.Val159Asp
ENST00000462494.5:n.1001T>A
ENST00000473257.1:n.194T>A
ENST00000477812.1:n.683T>A
ENST00000484841.5:n.631T>A
ENST00000493945.5:n.482T>A
NM_001101.3:c.476T>A , LRG_132t1:c.476T>A	NP_001092.1:p.Val159Asp
XM_006715764.1:c.110T>A	XP_006715827.1:p.Val37Asp
NM_001101.4:c.476T>A	NP_001092.1:p.Val159Asp
NM_001101.5:c.476T>A MANE Select	NP_001092.1:p.Val159Asp