Canonical Allele Identifier: CA2681649724

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528828-CTTGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528829_5528833del , CM000669.2:g.5528829_5528833del	GRCh38
NC_000007.13:g.5568460_5568464del , CM000669.1:g.5568460_5568464del	GRCh37
NC_000007.12:g.5534986_5534990del	NCBI36
NG_007992.1:g.6769_6773del , LRG_132:g.6769_6773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-114_364-110del	ENSP00000407473.2:n.364-114_364-110del
ENST00000473257.3:c.235-114_235-110del	ENSP00000501773.1:n.235-114_235-110del
ENST00000477812.2:n.797_801del
ENST00000484841.6:n.559-114_559-110del
ENST00000493945.6:c.364-114_364-110del	ENSP00000494269.1:n.364-114_364-110del
ENST00000642480.2:c.364-114_364-110del	ENSP00000495995.2:n.364-114_364-110del
ENST00000645576.1:c.364-162_364-158del	ENSP00000496101.1:n.364-162_364-158del
ENST00000646664.1:c.364-114_364-110del MANE Select	ENSP00000494750.1:n.364-114_364-110del
ENST00000647275.1:c.-3-114_-3-110del	ENSP00000494185.1:n.-3-114_-3-110del
ENST00000674681.1:c.364-114_364-110del	ENSP00000502821.1:n.364-114_364-110del
ENST00000675515.1:c.364-114_364-110del	ENSP00000501862.1:n.364-114_364-110del
ENST00000676189.1:c.375-126_375-122del	ENSP00000502538.1:n.375-126_375-122del
ENST00000676319.1:c.87+738_87+742del	ENSP00000502193.1:n.87+738_87+742del
ENST00000676397.1:c.364-114_364-110del	ENSP00000502286.1:n.364-114_364-110del
ENST00000331789.9:c.364-114_364-110del	ENSP00000349960.4:n.364-114_364-110del
ENST00000425660.5:c.*27-114_*27-110del	ENSP00000409264.1:n.*27-114_*27-110del
ENST00000432588.5:c.364-114_364-110del	ENSP00000407473.1:n.364-114_364-110del
ENST00000462494.5:n.775_779del
ENST00000473257.1:n.82-114_82-110del
ENST00000477812.1:n.571-114_571-110del
ENST00000484841.5:n.519-114_519-110del
ENST00000493945.5:n.370-114_370-110del
NM_001101.3:c.364-114_364-110del , LRG_132t1:c.364-114_364-110del	NP_001092.1:n.364-114_364-110del
XM_006715764.1:c.-117_-113del	XP_006715827.1:n.-117_-113del
NM_001101.4:c.364-114_364-110del	NP_001092.1:n.364-114_364-110del
NM_001101.5:c.364-114_364-110del MANE Select	NP_001092.1:n.364-114_364-110del