Canonical Allele Identifier: CA572822059

Gene: ACTB

Linked Data

• dbSNP Id: rs1562719494
• gnomAD v2: 7-5568604-GAC-G
• gnomAD v3: 7-5528973-GAC-G
• gnomAD v4: 7-5528973-GAC-G
• MyVariant Identifiers: chr7:g.5568605_5568606del (hg19) ; chr7:g.5528974_5528975del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528975_5528976del , CM000669.2:g.5528975_5528976del	GRCh38
NC_000007.13:g.5568606_5568607del , CM000669.1:g.5568606_5568607del	GRCh37
NC_000007.12:g.5535132_5535133del	NCBI36
NG_007992.1:g.6627_6628del , LRG_132:g.6627_6628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+186_363+187del	ENSP00000407473.2:n.363+186_363+187del
ENST00000473257.3:c.234+186_234+187del	ENSP00000501773.1:n.234+186_234+187del
ENST00000477812.2:n.655_656del
ENST00000484841.6:n.558+44_558+45del
ENST00000493945.6:c.363+186_363+187del	ENSP00000494269.1:n.363+186_363+187del
ENST00000642480.2:c.363+186_363+187del	ENSP00000495995.2:n.363+186_363+187del
ENST00000645025.1:n.531_532del
ENST00000645576.1:c.363+186_363+187del	ENSP00000496101.1:n.363+186_363+187del
ENST00000646664.1:c.363+186_363+187del MANE Select	ENSP00000494750.1:n.363+186_363+187del
ENST00000647275.1:c.-3-256_-3-255del	ENSP00000494185.1:n.-3-256_-3-255del
ENST00000674681.1:c.363+186_363+187del	ENSP00000502821.1:n.363+186_363+187del
ENST00000675515.1:c.363+186_363+187del	ENSP00000501862.1:n.363+186_363+187del
ENST00000676189.1:c.374+175_374+176del	ENSP00000502538.1:n.374+175_374+176del
ENST00000676319.1:c.87+596_87+597del	ENSP00000502193.1:n.87+596_87+597del
ENST00000676397.1:c.363+186_363+187del	ENSP00000502286.1:n.363+186_363+187del
ENST00000331789.9:c.363+186_363+187del	ENSP00000349960.4:n.363+186_363+187del
ENST00000425660.5:c.*26+44_*26+45del	ENSP00000409264.1:n.*26+44_*26+45del
ENST00000432588.5:c.363+186_363+187del	ENSP00000407473.1:n.363+186_363+187del
ENST00000462494.5:n.633_634del
ENST00000473257.1:n.82-256_82-255del
ENST00000477812.1:n.570+186_570+187del
ENST00000484841.5:n.518+186_518+187del
ENST00000493945.5:n.369+186_369+187del
NM_001101.3:c.363+186_363+187del , LRG_132t1:c.363+186_363+187del	NP_001092.1:n.363+186_363+187del
XM_006715764.1:c.-259_-258del	XP_006715827.1:n.-259_-258del
NM_001101.4:c.363+186_363+187del	NP_001092.1:n.363+186_363+187del
NM_001101.5:c.363+186_363+187del MANE Select	NP_001092.1:n.363+186_363+187del