Canonical Allele Identifier: CA2540843565

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528728_5528729del , CM000669.2:g.5528728_5528729del	GRCh38
NC_000007.13:g.5568359_5568360del , CM000669.1:g.5568359_5568360del	GRCh37
NC_000007.12:g.5534885_5534886del	NCBI36
NG_007992.1:g.6873_6874del , LRG_132:g.6873_6874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-10_364-9del	ENSP00000407473.2:n.364-10_364-9del
ENST00000473257.3:c.235-10_235-9del	ENSP00000501773.1:n.235-10_235-9del
ENST00000477812.2:n.901_902del
ENST00000484841.6:n.559-10_559-9del
ENST00000493945.6:c.364-10_364-9del	ENSP00000494269.1:n.364-10_364-9del
ENST00000642480.2:c.364-10_364-9del	ENSP00000495995.2:n.364-10_364-9del
ENST00000645576.1:c.364-58_364-57del	ENSP00000496101.1:n.364-58_364-57del
ENST00000646664.1:c.364-10_364-9del MANE Select	ENSP00000494750.1:n.364-10_364-9del
ENST00000647275.1:c.-3-10_-3-9del	ENSP00000494185.1:n.-3-10_-3-9del
ENST00000674681.1:c.364-10_364-9del	ENSP00000502821.1:n.364-10_364-9del
ENST00000675515.1:c.364-10_364-9del	ENSP00000501862.1:n.364-10_364-9del
ENST00000676189.1:c.375-22_375-21del	ENSP00000502538.1:n.375-22_375-21del
ENST00000676319.1:c.87+842_87+843del	ENSP00000502193.1:n.87+842_87+843del
ENST00000676397.1:c.364-10_364-9del	ENSP00000502286.1:n.364-10_364-9del
ENST00000331789.9:c.364-10_364-9del	ENSP00000349960.4:n.364-10_364-9del
ENST00000425660.5:c.*27-10_*27-9del	ENSP00000409264.1:n.*27-10_*27-9del
ENST00000432588.5:c.364-10_364-9del	ENSP00000407473.1:n.364-10_364-9del
ENST00000462494.5:n.879_880del
ENST00000473257.1:n.82-10_82-9del
ENST00000477812.1:n.571-10_571-9del
ENST00000484841.5:n.519-10_519-9del
ENST00000493945.5:n.370-10_370-9del
NM_001101.3:c.364-10_364-9del , LRG_132t1:c.364-10_364-9del	NP_001092.1:n.364-10_364-9del
XM_006715764.1:c.-13_-12del	XP_006715827.1:n.-13_-12del
NM_001101.4:c.364-10_364-9del	NP_001092.1:n.364-10_364-9del
NM_001101.5:c.364-10_364-9del MANE Select	NP_001092.1:n.364-10_364-9del