Canonical Allele Identifier: CA2570190292

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528739_5528740del , CM000669.2:g.5528739_5528740del	GRCh38
NC_000007.13:g.5568370_5568371del , CM000669.1:g.5568370_5568371del	GRCh37
NC_000007.12:g.5534896_5534897del	NCBI36
NG_007992.1:g.6862_6863del , LRG_132:g.6862_6863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-21_364-20del	ENSP00000407473.2:n.364-21_364-20del
ENST00000473257.3:c.235-21_235-20del	ENSP00000501773.1:n.235-21_235-20del
ENST00000477812.2:n.890_891del
ENST00000484841.6:n.559-21_559-20del
ENST00000493945.6:c.364-21_364-20del	ENSP00000494269.1:n.364-21_364-20del
ENST00000642480.2:c.364-21_364-20del	ENSP00000495995.2:n.364-21_364-20del
ENST00000645576.1:c.364-69_364-68del	ENSP00000496101.1:n.364-69_364-68del
ENST00000646664.1:c.364-21_364-20del MANE Select	ENSP00000494750.1:n.364-21_364-20del
ENST00000647275.1:c.-3-21_-3-20del	ENSP00000494185.1:n.-3-21_-3-20del
ENST00000674681.1:c.364-21_364-20del	ENSP00000502821.1:n.364-21_364-20del
ENST00000675515.1:c.364-21_364-20del	ENSP00000501862.1:n.364-21_364-20del
ENST00000676189.1:c.375-33_375-32del	ENSP00000502538.1:n.375-33_375-32del
ENST00000676319.1:c.87+831_87+832del	ENSP00000502193.1:n.87+831_87+832del
ENST00000676397.1:c.364-21_364-20del	ENSP00000502286.1:n.364-21_364-20del
ENST00000331789.9:c.364-21_364-20del	ENSP00000349960.4:n.364-21_364-20del
ENST00000425660.5:c.*27-21_*27-20del	ENSP00000409264.1:n.*27-21_*27-20del
ENST00000432588.5:c.364-21_364-20del	ENSP00000407473.1:n.364-21_364-20del
ENST00000462494.5:n.868_869del
ENST00000473257.1:n.82-21_82-20del
ENST00000477812.1:n.571-21_571-20del
ENST00000484841.5:n.519-21_519-20del
ENST00000493945.5:n.370-21_370-20del
NM_001101.3:c.364-21_364-20del , LRG_132t1:c.364-21_364-20del	NP_001092.1:n.364-21_364-20del
XM_006715764.1:c.-24_-23del	XP_006715827.1:n.-24_-23del
NM_001101.4:c.364-21_364-20del	NP_001092.1:n.364-21_364-20del
NM_001101.5:c.364-21_364-20del MANE Select	NP_001092.1:n.364-21_364-20del