Canonical Allele Identifier: CA366703937

Gene: ACTB

Linked Data

• dbSNP Id: rs1584262221
• MyVariant Identifiers: chr7:g.5568338T>G (hg19) ; chr7:g.5528707T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528707T>G , CM000669.2:g.5528707T>G	GRCh38
NC_000007.13:g.5568338T>G , CM000669.1:g.5568338T>G	GRCh37
NC_000007.12:g.5534864T>G	NCBI36
NG_007992.1:g.6895A>C , LRG_132:g.6895A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.376A>C	ENSP00000407473.2:p.Thr126Pro
ENST00000473257.3:c.247A>C	ENSP00000501773.1:p.Thr83Pro
ENST00000477812.2:n.923A>C
ENST00000493945.6:c.376A>C	ENSP00000494269.1:p.Thr126Pro
ENST00000642480.2:c.376A>C	ENSP00000495995.2:p.Thr126Pro
ENST00000645576.1:c.364-36A>C	ENSP00000496101.1:n.364-36A>C
ENST00000646664.1:c.376A>C MANE Select	ENSP00000494750.1:p.Thr126Pro
ENST00000647275.1:c.10A>C	ENSP00000494185.1:p.Thr4Pro
ENST00000674681.1:c.376A>C	ENSP00000502821.1:p.Thr126Pro
ENST00000675515.1:c.376A>C	ENSP00000501862.1:p.Thr126Pro
ENST00000676189.1:c.375A>C	ENSP00000502538.1:p.Pro125=
ENST00000676319.1:c.87+864A>C	ENSP00000502193.1:n.87+864A>C
ENST00000676397.1:c.376A>C	ENSP00000502286.1:p.Thr126Pro
ENST00000331789.9:c.376A>C	ENSP00000349960.4:p.Thr126Pro
ENST00000425660.5:c.*39A>C	ENSP00000409264.1:n.*39A>C
ENST00000432588.5:c.376A>C	ENSP00000407473.1:p.Thr126Pro
ENST00000462494.5:n.901A>C
ENST00000473257.1:n.94A>C
ENST00000477812.1:n.583A>C
ENST00000484841.5:n.531A>C
ENST00000493945.5:n.382A>C
NM_001101.3:c.376A>C , LRG_132t1:c.376A>C	NP_001092.1:p.Thr126Pro
XM_006715764.1:c.10A>C	XP_006715827.1:p.Thr4Pro
NM_001101.4:c.376A>C	NP_001092.1:p.Thr126Pro
NM_001101.5:c.376A>C MANE Select	NP_001092.1:p.Thr126Pro