Canonical Allele Identifier: CA453521354

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568819G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529188G>C , CM000669.2:g.5529188G>C	GRCh38
NC_000007.13:g.5568819G>C , CM000669.1:g.5568819G>C	GRCh37
NC_000007.12:g.5535345G>C	NCBI36
NG_007992.1:g.6414C>G , LRG_132:g.6414C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.336C>G	ENSP00000407473.2:p.Pro112=
ENST00000473257.3:c.207C>G	ENSP00000501773.1:p.Pro69=
ENST00000477812.2:n.543C>G
ENST00000484841.6:n.490C>G
ENST00000493945.6:c.336C>G	ENSP00000494269.1:p.Pro112=
ENST00000642480.2:c.336C>G	ENSP00000495995.2:p.Pro112=
ENST00000645025.1:n.419C>G
ENST00000645576.1:c.336C>G	ENSP00000496101.1:p.Pro112=
ENST00000646664.1:c.336C>G MANE Select	ENSP00000494750.1:p.Pro112=
ENST00000647275.1:c.-3-469C>G	ENSP00000494185.1:n.-3-469C>G
ENST00000674681.1:c.336C>G	ENSP00000502821.1:p.Pro112=
ENST00000675515.1:c.336C>G	ENSP00000501862.1:p.Pro112=
ENST00000676189.1:c.336C>G	ENSP00000502538.1:p.Pro112=
ENST00000676319.1:c.87+383C>G	ENSP00000502193.1:n.87+383C>G
ENST00000676397.1:c.336C>G	ENSP00000502286.1:p.Pro112=
ENST00000331789.9:c.336C>G	ENSP00000349960.4:p.Pro112=
ENST00000425660.5:c.336C>G	ENSP00000409264.1:p.Pro112=
ENST00000432588.5:c.336C>G	ENSP00000407473.1:p.Pro112=
ENST00000462494.5:n.420C>G
ENST00000473257.1:n.82-469C>G
ENST00000477812.1:n.543C>G
ENST00000480301.1:n.536C>G
ENST00000484841.5:n.491C>G
ENST00000493945.5:n.342C>G
NM_001101.3:c.336C>G , LRG_132t1:c.336C>G	NP_001092.1:p.Pro112=
XM_006715764.1:c.-371C>G	XP_006715827.1:n.-371C>G
NM_001101.4:c.336C>G	NP_001092.1:p.Pro112=
NM_001101.5:c.336C>G MANE Select	NP_001092.1:p.Pro112=