Canonical Allele Identifier: CA2681649829

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528912-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528912G>C , CM000669.2:g.5528912G>C	GRCh38
NC_000007.13:g.5568543G>C , CM000669.1:g.5568543G>C	GRCh37
NC_000007.12:g.5535069G>C	NCBI36
NG_007992.1:g.6690C>G , LRG_132:g.6690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-193C>G	ENSP00000407473.2:n.364-193C>G
ENST00000473257.3:c.235-193C>G	ENSP00000501773.1:n.235-193C>G
ENST00000477812.2:n.718C>G
ENST00000484841.6:n.558+107C>G
ENST00000493945.6:c.364-193C>G	ENSP00000494269.1:n.364-193C>G
ENST00000642480.2:c.364-193C>G	ENSP00000495995.2:n.364-193C>G
ENST00000645576.1:c.364-241C>G	ENSP00000496101.1:n.364-241C>G
ENST00000646664.1:c.364-193C>G MANE Select	ENSP00000494750.1:n.364-193C>G
ENST00000647275.1:c.-3-193C>G	ENSP00000494185.1:n.-3-193C>G
ENST00000674681.1:c.364-193C>G	ENSP00000502821.1:n.364-193C>G
ENST00000675515.1:c.364-193C>G	ENSP00000501862.1:n.364-193C>G
ENST00000676189.1:c.375-205C>G	ENSP00000502538.1:n.375-205C>G
ENST00000676319.1:c.87+659C>G	ENSP00000502193.1:n.87+659C>G
ENST00000676397.1:c.364-193C>G	ENSP00000502286.1:n.364-193C>G
ENST00000331789.9:c.364-193C>G	ENSP00000349960.4:n.364-193C>G
ENST00000425660.5:c.*26+107C>G	ENSP00000409264.1:n.*26+107C>G
ENST00000432588.5:c.364-193C>G	ENSP00000407473.1:n.364-193C>G
ENST00000462494.5:n.696C>G
ENST00000473257.1:n.82-193C>G
ENST00000477812.1:n.571-193C>G
ENST00000484841.5:n.519-193C>G
ENST00000493945.5:n.370-193C>G
NM_001101.3:c.364-193C>G , LRG_132t1:c.364-193C>G	NP_001092.1:n.364-193C>G
XM_006715764.1:c.-196C>G	XP_006715827.1:n.-196C>G
NM_001101.4:c.364-193C>G	NP_001092.1:n.364-193C>G
NM_001101.5:c.364-193C>G MANE Select	NP_001092.1:n.364-193C>G