Canonical Allele Identifier: CA366702035

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568001T>G (hg19) ; chr7:g.5528370T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528370T>G , CM000669.2:g.5528370T>G	GRCh38
NC_000007.13:g.5568001T>G , CM000669.1:g.5568001T>G	GRCh37
NC_000007.12:g.5534527T>G	NCBI36
NG_007992.1:g.7232A>C , LRG_132:g.7232A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.713A>C	ENSP00000407473.2:p.Lys238Thr
ENST00000473257.3:c.584A>C	ENSP00000501773.1:p.Lys195Thr
ENST00000477812.2:n.1260A>C
ENST00000493945.6:c.713A>C	ENSP00000494269.1:p.Lys238Thr
ENST00000642480.2:c.713A>C	ENSP00000495995.2:p.Lys238Thr
ENST00000645576.1:c.665A>C	ENSP00000496101.1:p.Lys222Thr
ENST00000646664.1:c.713A>C MANE Select	ENSP00000494750.1:p.Lys238Thr
ENST00000647275.1:c.347A>C	ENSP00000494185.1:p.Lys116Thr
ENST00000674681.1:c.713A>C	ENSP00000502821.1:p.Lys238Thr
ENST00000675515.1:c.713A>C	ENSP00000501862.1:p.Lys238Thr
ENST00000676189.1:c.*256A>C	ENSP00000502538.1:n.*256A>C
ENST00000676319.1:c.88-587A>C	ENSP00000502193.1:n.88-587A>C
ENST00000676397.1:c.713A>C	ENSP00000502286.1:p.Lys238Thr
ENST00000331789.9:c.713A>C	ENSP00000349960.4:p.Lys238Thr
ENST00000425660.5:c.*376A>C	ENSP00000409264.1:n.*376A>C
ENST00000462494.5:n.1238A>C
ENST00000473257.1:n.431A>C
ENST00000484841.5:n.868A>C
ENST00000493945.5:n.719A>C
NM_001101.3:c.713A>C , LRG_132t1:c.713A>C	NP_001092.1:p.Lys238Thr
XM_006715764.1:c.347A>C	XP_006715827.1:p.Lys116Thr
NM_001101.4:c.713A>C	NP_001092.1:p.Lys238Thr
NM_001101.5:c.713A>C MANE Select	NP_001092.1:p.Lys238Thr