Canonical Allele Identifier: CA366702680

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568136A>G (hg19) ; chr7:g.5528505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528505A>G , CM000669.2:g.5528505A>G	GRCh38
NC_000007.13:g.5568136A>G , CM000669.1:g.5568136A>G	GRCh37
NC_000007.12:g.5534662A>G	NCBI36
NG_007992.1:g.7097T>C , LRG_132:g.7097T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.578T>C	ENSP00000407473.2:p.Leu193Pro
ENST00000473257.3:c.449T>C	ENSP00000501773.1:p.Leu150Pro
ENST00000477812.2:n.1125T>C
ENST00000493945.6:c.578T>C	ENSP00000494269.1:p.Leu193Pro
ENST00000642480.2:c.578T>C	ENSP00000495995.2:p.Leu193Pro
ENST00000645576.1:c.530T>C	ENSP00000496101.1:p.Leu177Pro
ENST00000646664.1:c.578T>C MANE Select	ENSP00000494750.1:p.Leu193Pro
ENST00000647275.1:c.212T>C	ENSP00000494185.1:p.Leu71Pro
ENST00000674681.1:c.578T>C	ENSP00000502821.1:p.Leu193Pro
ENST00000675515.1:c.578T>C	ENSP00000501862.1:p.Leu193Pro
ENST00000676189.1:c.*121T>C	ENSP00000502538.1:n.*121T>C
ENST00000676319.1:c.88-722T>C	ENSP00000502193.1:n.88-722T>C
ENST00000676397.1:c.578T>C	ENSP00000502286.1:p.Leu193Pro
ENST00000331789.9:c.578T>C	ENSP00000349960.4:p.Leu193Pro
ENST00000425660.5:c.*241T>C	ENSP00000409264.1:n.*241T>C
ENST00000462494.5:n.1103T>C
ENST00000473257.1:n.296T>C
ENST00000477812.1:n.785T>C
ENST00000484841.5:n.733T>C
ENST00000493945.5:n.584T>C
NM_001101.3:c.578T>C , LRG_132t1:c.578T>C	NP_001092.1:p.Leu193Pro
XM_006715764.1:c.212T>C	XP_006715827.1:p.Leu71Pro
NM_001101.4:c.578T>C	NP_001092.1:p.Leu193Pro
NM_001101.5:c.578T>C MANE Select	NP_001092.1:p.Leu193Pro