Canonical Allele Identifier: CA366703496

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568244T>G (hg19) ; chr7:g.5528613T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528613T>G , CM000669.2:g.5528613T>G	GRCh38
NC_000007.13:g.5568244T>G , CM000669.1:g.5568244T>G	GRCh37
NC_000007.12:g.5534770T>G	NCBI36
NG_007992.1:g.6989A>C , LRG_132:g.6989A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.470A>C	ENSP00000407473.2:p.Asp157Ala
ENST00000473257.3:c.341A>C	ENSP00000501773.1:p.Asp114Ala
ENST00000477812.2:n.1017A>C
ENST00000493945.6:c.470A>C	ENSP00000494269.1:p.Asp157Ala
ENST00000642480.2:c.470A>C	ENSP00000495995.2:p.Asp157Ala
ENST00000645576.1:c.422A>C	ENSP00000496101.1:p.Asp141Ala
ENST00000646664.1:c.470A>C MANE Select	ENSP00000494750.1:p.Asp157Ala
ENST00000647275.1:c.104A>C	ENSP00000494185.1:p.Asp35Ala
ENST00000674681.1:c.470A>C	ENSP00000502821.1:p.Asp157Ala
ENST00000675515.1:c.470A>C	ENSP00000501862.1:p.Asp157Ala
ENST00000676189.1:c.*13A>C	ENSP00000502538.1:n.*13A>C
ENST00000676319.1:c.88-830A>C	ENSP00000502193.1:n.88-830A>C
ENST00000676397.1:c.470A>C	ENSP00000502286.1:p.Asp157Ala
ENST00000331789.9:c.470A>C	ENSP00000349960.4:p.Asp157Ala
ENST00000425660.5:c.*133A>C	ENSP00000409264.1:n.*133A>C
ENST00000432588.5:c.470A>C	ENSP00000407473.1:p.Asp157Ala
ENST00000462494.5:n.995A>C
ENST00000473257.1:n.188A>C
ENST00000477812.1:n.677A>C
ENST00000484841.5:n.625A>C
ENST00000493945.5:n.476A>C
NM_001101.3:c.470A>C , LRG_132t1:c.470A>C	NP_001092.1:p.Asp157Ala
XM_006715764.1:c.104A>C	XP_006715827.1:p.Asp35Ala
NM_001101.4:c.470A>C	NP_001092.1:p.Asp157Ala
NM_001101.5:c.470A>C MANE Select	NP_001092.1:p.Asp157Ala