Canonical Allele Identifier: CA153195620

Gene: ACTB

Linked Data

• ClinVar Variation Id: 1567407
• ClinVar RCV Id: RCV002214810
• dbSNP Id: rs760547214
• gnomAD v2: 7-5568249-G-A
• gnomAD v3: 7-5528618-G-A
• gnomAD v4: 7-5528618-G-A
• COSMIC: COSM3266901
• MyVariant Identifiers: chr7:g.5568249G>A (hg19) ; chr7:g.5528618G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528618G>A , CM000669.2:g.5528618G>A	GRCh38
NC_000007.13:g.5568249G>A , CM000669.1:g.5568249G>A	GRCh37
NC_000007.12:g.5534775G>A	NCBI36
NG_007992.1:g.6984C>T , LRG_132:g.6984C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.465C>T	ENSP00000407473.2:p.Ser155=
ENST00000473257.3:c.336C>T	ENSP00000501773.1:p.Ser112=
ENST00000477812.2:n.1012C>T
ENST00000493945.6:c.465C>T	ENSP00000494269.1:p.Ser155=
ENST00000642480.2:c.465C>T	ENSP00000495995.2:p.Ser155=
ENST00000645576.1:c.417C>T	ENSP00000496101.1:p.Ser139=
ENST00000646664.1:c.465C>T MANE Select	ENSP00000494750.1:p.Ser155=
ENST00000647275.1:c.99C>T	ENSP00000494185.1:p.Ser33=
ENST00000674681.1:c.465C>T	ENSP00000502821.1:p.Ser155=
ENST00000675515.1:c.465C>T	ENSP00000501862.1:p.Ser155=
ENST00000676189.1:c.*8C>T	ENSP00000502538.1:n.*8C>T
ENST00000676319.1:c.88-835C>T	ENSP00000502193.1:n.88-835C>T
ENST00000676397.1:c.465C>T	ENSP00000502286.1:p.Ser155=
ENST00000331789.9:c.465C>T	ENSP00000349960.4:p.Ser155=
ENST00000425660.5:c.*128C>T	ENSP00000409264.1:n.*128C>T
ENST00000432588.5:c.465C>T	ENSP00000407473.1:p.Ser155=
ENST00000462494.5:n.990C>T
ENST00000473257.1:n.183C>T
ENST00000477812.1:n.672C>T
ENST00000484841.5:n.620C>T
ENST00000493945.5:n.471C>T
NM_001101.3:c.465C>T , LRG_132t1:c.465C>T	NP_001092.1:p.Ser155=
XM_006715764.1:c.99C>T	XP_006715827.1:p.Ser33=
NM_001101.4:c.465C>T	NP_001092.1:p.Ser155=
NM_001101.5:c.465C>T MANE Select	NP_001092.1:p.Ser155=