Canonical Allele Identifier: CA366703512

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568248C>A (hg19) ; chr7:g.5528617C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528617C>A , CM000669.2:g.5528617C>A	GRCh38
NC_000007.13:g.5568248C>A , CM000669.1:g.5568248C>A	GRCh37
NC_000007.12:g.5534774C>A	NCBI36
NG_007992.1:g.6985G>T , LRG_132:g.6985G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.466G>T	ENSP00000407473.2:p.Gly156Cys
ENST00000473257.3:c.337G>T	ENSP00000501773.1:p.Gly113Cys
ENST00000477812.2:n.1013G>T
ENST00000493945.6:c.466G>T	ENSP00000494269.1:p.Gly156Cys
ENST00000642480.2:c.466G>T	ENSP00000495995.2:p.Gly156Cys
ENST00000645576.1:c.418G>T	ENSP00000496101.1:p.Gly140Cys
ENST00000646664.1:c.466G>T MANE Select	ENSP00000494750.1:p.Gly156Cys
ENST00000647275.1:c.100G>T	ENSP00000494185.1:p.Gly34Cys
ENST00000674681.1:c.466G>T	ENSP00000502821.1:p.Gly156Cys
ENST00000675515.1:c.466G>T	ENSP00000501862.1:p.Gly156Cys
ENST00000676189.1:c.*9G>T	ENSP00000502538.1:n.*9G>T
ENST00000676319.1:c.88-834G>T	ENSP00000502193.1:n.88-834G>T
ENST00000676397.1:c.466G>T	ENSP00000502286.1:p.Gly156Cys
ENST00000331789.9:c.466G>T	ENSP00000349960.4:p.Gly156Cys
ENST00000425660.5:c.*129G>T	ENSP00000409264.1:n.*129G>T
ENST00000432588.5:c.466G>T	ENSP00000407473.1:p.Gly156Cys
ENST00000462494.5:n.991G>T
ENST00000473257.1:n.184G>T
ENST00000477812.1:n.673G>T
ENST00000484841.5:n.621G>T
ENST00000493945.5:n.472G>T
NM_001101.3:c.466G>T , LRG_132t1:c.466G>T	NP_001092.1:p.Gly156Cys
XM_006715764.1:c.100G>T	XP_006715827.1:p.Gly34Cys
NM_001101.4:c.466G>T	NP_001092.1:p.Gly156Cys
NM_001101.5:c.466G>T MANE Select	NP_001092.1:p.Gly156Cys