Canonical Allele Identifier: CA2681649669

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528761-TGGGGACAGCCAGGCCAGACG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528769_5528788del , CM000669.2:g.5528769_5528788del	GRCh38
NC_000007.13:g.5568400_5568419del , CM000669.1:g.5568400_5568419del	GRCh37
NC_000007.12:g.5534926_5534945del	NCBI36
NG_007992.1:g.6821_6840del , LRG_132:g.6821_6840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-62_364-43del	ENSP00000407473.2:n.364-62_364-43del
ENST00000473257.3:c.235-62_235-43del	ENSP00000501773.1:n.235-62_235-43del
ENST00000477812.2:n.849_868del
ENST00000484841.6:n.559-62_559-43del
ENST00000493945.6:c.364-62_364-43del	ENSP00000494269.1:n.364-62_364-43del
ENST00000642480.2:c.364-62_364-43del	ENSP00000495995.2:n.364-62_364-43del
ENST00000645576.1:c.364-110_364-91del	ENSP00000496101.1:n.364-110_364-91del
ENST00000646664.1:c.364-62_364-43del MANE Select	ENSP00000494750.1:n.364-62_364-43del
ENST00000647275.1:c.-3-62_-3-43del	ENSP00000494185.1:n.-3-62_-3-43del
ENST00000674681.1:c.364-62_364-43del	ENSP00000502821.1:n.364-62_364-43del
ENST00000675515.1:c.364-62_364-43del	ENSP00000501862.1:n.364-62_364-43del
ENST00000676189.1:c.375-74_375-55del	ENSP00000502538.1:n.375-74_375-55del
ENST00000676319.1:c.87+790_87+809del	ENSP00000502193.1:n.87+790_87+809del
ENST00000676397.1:c.364-62_364-43del	ENSP00000502286.1:n.364-62_364-43del
ENST00000331789.9:c.364-62_364-43del	ENSP00000349960.4:n.364-62_364-43del
ENST00000425660.5:c.*27-62_*27-43del	ENSP00000409264.1:n.*27-62_*27-43del
ENST00000432588.5:c.364-62_364-43del	ENSP00000407473.1:n.364-62_364-43del
ENST00000462494.5:n.827_846del
ENST00000473257.1:n.82-62_82-43del
ENST00000477812.1:n.571-62_571-43del
ENST00000484841.5:n.519-62_519-43del
ENST00000493945.5:n.370-62_370-43del
NM_001101.3:c.364-62_364-43del , LRG_132t1:c.364-62_364-43del	NP_001092.1:n.364-62_364-43del
XM_006715764.1:c.-65_-46del	XP_006715827.1:n.-65_-46del
NM_001101.4:c.364-62_364-43del	NP_001092.1:n.364-62_364-43del
NM_001101.5:c.364-62_364-43del MANE Select	NP_001092.1:n.364-62_364-43del