Canonical Allele Identifier: CA366703508

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568247C>G (hg19) ; chr7:g.5528616C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528616C>G , CM000669.2:g.5528616C>G	GRCh38
NC_000007.13:g.5568247C>G , CM000669.1:g.5568247C>G	GRCh37
NC_000007.12:g.5534773C>G	NCBI36
NG_007992.1:g.6986G>C , LRG_132:g.6986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.467G>C	ENSP00000407473.2:p.Gly156Ala
ENST00000473257.3:c.338G>C	ENSP00000501773.1:p.Gly113Ala
ENST00000477812.2:n.1014G>C
ENST00000493945.6:c.467G>C	ENSP00000494269.1:p.Gly156Ala
ENST00000642480.2:c.467G>C	ENSP00000495995.2:p.Gly156Ala
ENST00000645576.1:c.419G>C	ENSP00000496101.1:p.Gly140Ala
ENST00000646664.1:c.467G>C MANE Select	ENSP00000494750.1:p.Gly156Ala
ENST00000647275.1:c.101G>C	ENSP00000494185.1:p.Gly34Ala
ENST00000674681.1:c.467G>C	ENSP00000502821.1:p.Gly156Ala
ENST00000675515.1:c.467G>C	ENSP00000501862.1:p.Gly156Ala
ENST00000676189.1:c.*10G>C	ENSP00000502538.1:n.*10G>C
ENST00000676319.1:c.88-833G>C	ENSP00000502193.1:n.88-833G>C
ENST00000676397.1:c.467G>C	ENSP00000502286.1:p.Gly156Ala
ENST00000331789.9:c.467G>C	ENSP00000349960.4:p.Gly156Ala
ENST00000425660.5:c.*130G>C	ENSP00000409264.1:n.*130G>C
ENST00000432588.5:c.467G>C	ENSP00000407473.1:p.Gly156Ala
ENST00000462494.5:n.992G>C
ENST00000473257.1:n.185G>C
ENST00000477812.1:n.674G>C
ENST00000484841.5:n.622G>C
ENST00000493945.5:n.473G>C
NM_001101.3:c.467G>C , LRG_132t1:c.467G>C	NP_001092.1:p.Gly156Ala
XM_006715764.1:c.101G>C	XP_006715827.1:p.Gly34Ala
NM_001101.4:c.467G>C	NP_001092.1:p.Gly156Ala
NM_001101.5:c.467G>C MANE Select	NP_001092.1:p.Gly156Ala