Canonical Allele Identifier: CA453639162

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568237G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528606G>C , CM000669.2:g.5528606G>C	GRCh38
NC_000007.13:g.5568237G>C , CM000669.1:g.5568237G>C	GRCh37
NC_000007.12:g.5534763G>C	NCBI36
NG_007992.1:g.6996C>G , LRG_132:g.6996C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.477C>G	ENSP00000407473.2:p.Val159=
ENST00000473257.3:c.348C>G	ENSP00000501773.1:p.Val116=
ENST00000477812.2:n.1024C>G
ENST00000493945.6:c.477C>G	ENSP00000494269.1:p.Val159=
ENST00000642480.2:c.477C>G	ENSP00000495995.2:p.Val159=
ENST00000645576.1:c.429C>G	ENSP00000496101.1:p.Val143=
ENST00000646664.1:c.477C>G MANE Select	ENSP00000494750.1:p.Val159=
ENST00000647275.1:c.111C>G	ENSP00000494185.1:p.Val37=
ENST00000674681.1:c.477C>G	ENSP00000502821.1:p.Val159=
ENST00000675515.1:c.477C>G	ENSP00000501862.1:p.Val159=
ENST00000676189.1:c.*20C>G	ENSP00000502538.1:n.*20C>G
ENST00000676319.1:c.88-823C>G	ENSP00000502193.1:n.88-823C>G
ENST00000676397.1:c.477C>G	ENSP00000502286.1:p.Val159=
ENST00000331789.9:c.477C>G	ENSP00000349960.4:p.Val159=
ENST00000425660.5:c.*140C>G	ENSP00000409264.1:n.*140C>G
ENST00000432588.5:c.477C>G	ENSP00000407473.1:p.Val159=
ENST00000462494.5:n.1002C>G
ENST00000473257.1:n.195C>G
ENST00000477812.1:n.684C>G
ENST00000484841.5:n.632C>G
ENST00000493945.5:n.483C>G
NM_001101.3:c.477C>G , LRG_132t1:c.477C>G	NP_001092.1:p.Val159=
XM_006715764.1:c.111C>G	XP_006715827.1:p.Val37=
NM_001101.4:c.477C>G	NP_001092.1:p.Val159=
NM_001101.5:c.477C>G MANE Select	NP_001092.1:p.Val159=