Canonical Allele Identifier: CA1097928487

Gene: ACTB

Linked Data

• gnomAD v3: 7-5528577-TAC-T
• gnomAD v4: 7-5528577-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528578_5528579del , CM000669.2:g.5528578_5528579del	GRCh38
NC_000007.13:g.5568209_5568210del , CM000669.1:g.5568209_5568210del	GRCh37
NC_000007.12:g.5534735_5534736del	NCBI36
NG_007992.1:g.7023_7024del , LRG_132:g.7023_7024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.504_505del	ENSP00000407473.2:p.Tyr169CysfsTer18
ENST00000473257.3:c.375_376del	ENSP00000501773.1:p.Tyr126CysfsTer18
ENST00000477812.2:n.1051_1052del
ENST00000493945.6:c.504_505del	ENSP00000494269.1:p.Tyr169CysfsTer18
ENST00000642480.2:c.504_505del	ENSP00000495995.2:p.Tyr169CysfsTer18
ENST00000645576.1:c.456_457del	ENSP00000496101.1:p.Tyr153CysfsTer18
ENST00000646664.1:c.504_505del MANE Select	ENSP00000494750.1:p.Tyr169CysfsTer18
ENST00000647275.1:c.138_139del	ENSP00000494185.1:p.Tyr47CysfsTer18
ENST00000674681.1:c.504_505del	ENSP00000502821.1:p.Tyr169CysfsTer18
ENST00000675515.1:c.504_505del	ENSP00000501862.1:p.Tyr169CysfsTer18
ENST00000676189.1:c.*47_*48del	ENSP00000502538.1:n.*47_*48del
ENST00000676319.1:c.88-796_88-795del	ENSP00000502193.1:n.88-796_88-795del
ENST00000676397.1:c.504_505del	ENSP00000502286.1:p.Tyr169CysfsTer18
ENST00000331789.9:c.504_505del	ENSP00000349960.4:p.Tyr169CysfsTer18
ENST00000425660.5:c.*167_*168del	ENSP00000409264.1:n.*167_*168del
ENST00000462494.5:n.1029_1030del
ENST00000473257.1:n.222_223del
ENST00000477812.1:n.711_712del
ENST00000484841.5:n.659_660del
ENST00000493945.5:n.510_511del
NM_001101.3:c.504_505del , LRG_132t1:c.504_505del	NP_001092.1:p.Tyr169CysfsTer18
XM_006715764.1:c.138_139del	XP_006715827.1:p.Tyr47CysfsTer18
NM_001101.4:c.504_505del	NP_001092.1:p.Tyr169CysfsTer18
NM_001101.5:c.504_505del MANE Select	NP_001092.1:p.Tyr169CysfsTer18