Canonical Allele Identifier: CA572822060

Gene: ACTB

Linked Data

• dbSNP Id: rs1425000269
• gnomAD v2: 7-5568605-AC-A
• gnomAD v3: 7-5528974-AC-A
• gnomAD v4: 7-5528974-AC-A
• MyVariant Identifiers: chr7:g.5568606del (hg19) ; chr7:g.5528975del (hg38)

Genomic Alleles

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

Transcript Alleles

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