Canonical Allele Identifier: CA1097928606

Gene: ACTB

Linked Data

• dbSNP Id: rs1235987665
• gnomAD v3: 7-5528745-ACACTGGGGAAGC-A
• gnomAD v4: 7-5528745-ACACTGGGGAAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528755_5528766del , CM000669.2:g.5528755_5528766del	GRCh38
NC_000007.13:g.5568386_5568397del , CM000669.1:g.5568386_5568397del	GRCh37
NC_000007.12:g.5534912_5534923del	NCBI36
NG_007992.1:g.6845_6856del , LRG_132:g.6845_6856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-38_364-27del	ENSP00000407473.2:n.364-38_364-27del
ENST00000473257.3:c.235-38_235-27del	ENSP00000501773.1:n.235-38_235-27del
ENST00000477812.2:n.873_884del
ENST00000484841.6:n.559-38_559-27del
ENST00000493945.6:c.364-38_364-27del	ENSP00000494269.1:n.364-38_364-27del
ENST00000642480.2:c.364-38_364-27del	ENSP00000495995.2:n.364-38_364-27del
ENST00000645576.1:c.364-86_364-75del	ENSP00000496101.1:n.364-86_364-75del
ENST00000646664.1:c.364-38_364-27del MANE Select	ENSP00000494750.1:n.364-38_364-27del
ENST00000647275.1:c.-3-38_-3-27del	ENSP00000494185.1:n.-3-38_-3-27del
ENST00000674681.1:c.364-38_364-27del	ENSP00000502821.1:n.364-38_364-27del
ENST00000675515.1:c.364-38_364-27del	ENSP00000501862.1:n.364-38_364-27del
ENST00000676189.1:c.375-50_375-39del	ENSP00000502538.1:n.375-50_375-39del
ENST00000676319.1:c.87+814_87+825del	ENSP00000502193.1:n.87+814_87+825del
ENST00000676397.1:c.364-38_364-27del	ENSP00000502286.1:n.364-38_364-27del
ENST00000331789.9:c.364-38_364-27del	ENSP00000349960.4:n.364-38_364-27del
ENST00000425660.5:c.*27-38_*27-27del	ENSP00000409264.1:n.*27-38_*27-27del
ENST00000432588.5:c.364-38_364-27del	ENSP00000407473.1:n.364-38_364-27del
ENST00000462494.5:n.851_862del
ENST00000473257.1:n.82-38_82-27del
ENST00000477812.1:n.571-38_571-27del
ENST00000484841.5:n.519-38_519-27del
ENST00000493945.5:n.370-38_370-27del
NM_001101.3:c.364-38_364-27del , LRG_132t1:c.364-38_364-27del	NP_001092.1:n.364-38_364-27del
XM_006715764.1:c.-41_-30del	XP_006715827.1:n.-41_-30del
NM_001101.4:c.364-38_364-27del	NP_001092.1:n.364-38_364-27del
NM_001101.5:c.364-38_364-27del MANE Select	NP_001092.1:n.364-38_364-27del