Canonical Allele Identifier: CA2740813913

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529076A>C , CM000669.2:g.5529076A>C	GRCh38
NC_000007.13:g.5568707A>C , CM000669.1:g.5568707A>C	GRCh37
NC_000007.12:g.5535233A>C	NCBI36
NG_007992.1:g.6526T>G , LRG_132:g.6526T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.363+85T>G	ENSP00000407473.2:n.363+85T>G
ENST00000473257.3:c.234+85T>G	ENSP00000501773.1:n.234+85T>G
ENST00000477812.2:n.571-17T>G
ENST00000484841.6:n.518-17T>G
ENST00000493945.6:c.363+85T>G	ENSP00000494269.1:n.363+85T>G
ENST00000642480.2:c.363+85T>G	ENSP00000495995.2:n.363+85T>G
ENST00000645025.1:n.447-17T>G
ENST00000645576.1:c.363+85T>G	ENSP00000496101.1:n.363+85T>G
ENST00000646664.1:c.363+85T>G MANE Select	ENSP00000494750.1:n.363+85T>G
ENST00000647275.1:c.-3-357T>G	ENSP00000494185.1:n.-3-357T>G
ENST00000674681.1:c.363+85T>G	ENSP00000502821.1:n.363+85T>G
ENST00000675515.1:c.363+85T>G	ENSP00000501862.1:n.363+85T>G
ENST00000676189.1:c.374+74T>G	ENSP00000502538.1:n.374+74T>G
ENST00000676319.1:c.87+495T>G	ENSP00000502193.1:n.87+495T>G
ENST00000676397.1:c.363+85T>G	ENSP00000502286.1:n.363+85T>G
ENST00000331789.9:c.363+85T>G	ENSP00000349960.4:n.363+85T>G
ENST00000425660.5:c.364-17T>G	ENSP00000409264.1:n.364-17T>G
ENST00000432588.5:c.363+85T>G	ENSP00000407473.1:n.363+85T>G
ENST00000462494.5:n.532T>G
ENST00000473257.1:n.82-357T>G
ENST00000477812.1:n.570+85T>G
ENST00000480301.1:n.648T>G
ENST00000484841.5:n.518+85T>G
ENST00000493945.5:n.369+85T>G
NM_001101.3:c.363+85T>G , LRG_132t1:c.363+85T>G	NP_001092.1:n.363+85T>G
XM_006715764.1:c.-343-17T>G	XP_006715827.1:n.-343-17T>G
NM_001101.4:c.363+85T>G	NP_001092.1:n.363+85T>G
NM_001101.5:c.363+85T>G MANE Select	NP_001092.1:n.363+85T>G