Canonical Allele Identifier: CA1684976425

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528967_5528969delinsCAG , CM000669.2:g.5528967_5528969delinsCAG	GRCh38
NC_000007.13:g.5568598_5568600delinsCAG , CM000669.1:g.5568598_5568600delinsCAG	GRCh37
NC_000007.12:g.5535124_5535126delinsCAG	NCBI36
NG_007992.1:g.6633_6635delinsCTG , LRG_132:g.6633_6635delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+192_363+194delinsCTG	ENSP00000407473.2:n.363+192_363+194delinsCTG
ENST00000473257.3:c.234+192_234+194delinsCTG	ENSP00000501773.1:n.234+192_234+194delinsCTG
ENST00000477812.2:n.661_663delinsCTG
ENST00000484841.6:n.558+50_558+52delinsCTG
ENST00000493945.6:c.363+192_363+194delinsCTG	ENSP00000494269.1:n.363+192_363+194delinsCTG
ENST00000642480.2:c.363+192_363+194delinsCTG	ENSP00000495995.2:n.363+192_363+194delinsCTG
ENST00000645025.1:n.537_539delinsCTG
ENST00000645576.1:c.363+192_363+194delinsCTG	ENSP00000496101.1:n.363+192_363+194delinsCTG
ENST00000646664.1:c.363+192_363+194delinsCTG MANE Select	ENSP00000494750.1:n.363+192_363+194delinsCTG
ENST00000647275.1:c.-3-250_-3-248delinsCTG	ENSP00000494185.1:n.-3-250_-3-248delinsCTG
ENST00000674681.1:c.363+192_363+194delinsCTG	ENSP00000502821.1:n.363+192_363+194delinsCTG
ENST00000675515.1:c.363+192_363+194delinsCTG	ENSP00000501862.1:n.363+192_363+194delinsCTG
ENST00000676189.1:c.374+181_374+183delinsCTG	ENSP00000502538.1:n.374+181_374+183delinsCTG
ENST00000676319.1:c.87+602_87+604delinsCTG	ENSP00000502193.1:n.87+602_87+604delinsCTG
ENST00000676397.1:c.363+192_363+194delinsCTG	ENSP00000502286.1:n.363+192_363+194delinsCTG
ENST00000331789.9:c.363+192_363+194delinsCTG	ENSP00000349960.4:n.363+192_363+194delinsCTG
ENST00000425660.5:c.*26+50_*26+52delinsCTG	ENSP00000409264.1:n.*26+50_*26+52delinsCTG
ENST00000432588.5:c.363+192_363+194delinsCTG	ENSP00000407473.1:n.363+192_363+194delinsCTG
ENST00000462494.5:n.639_641delinsCTG
ENST00000473257.1:n.82-250_82-248delinsCTG
ENST00000477812.1:n.570+192_570+194delinsCTG
ENST00000484841.5:n.518+192_518+194delinsCTG
ENST00000493945.5:n.369+192_369+194delinsCTG
NM_001101.3:c.363+192_363+194delinsCTG , LRG_132t1:c.363+192_363+194delinsCTG	NP_001092.1:n.363+192_363+194delinsCTG
XM_006715764.1:c.-253_-251delinsCTG	XP_006715827.1:n.-253_-251delinsCTG
NM_001101.4:c.363+192_363+194delinsCTG	NP_001092.1:n.363+192_363+194delinsCTG
NM_001101.5:c.363+192_363+194delinsCTG MANE Select	NP_001092.1:n.363+192_363+194delinsCTG