Canonical Allele Identifier: CA1684975972

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528745_5528757delinsACACTGGGGAAGC , CM000669.2:g.5528745_5528757delinsACACTGGGGAAGC	GRCh38
NC_000007.13:g.5568376_5568388delinsACACTGGGGAAGC , CM000669.1:g.5568376_5568388delinsACACTGGGGAAGC	GRCh37
NC_000007.12:g.5534902_5534914delinsACACTGGGGAAGC	NCBI36
NG_007992.1:g.6845_6857delinsGCTTCCCCAGTGT , LRG_132:g.6845_6857delinsGCTTCCCCAGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000407473.2:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000473257.3:c.235-38_235-26delinsGCTTCCCCAGTGT	ENSP00000501773.1:n.235-38_235-26delinsGCTTCCCCAGTGT
ENST00000477812.2:n.873_885delinsGCTTCCCCAGTGT
ENST00000484841.6:n.559-38_559-26delinsGCTTCCCCAGTGT
ENST00000493945.6:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000494269.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000642480.2:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000495995.2:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000645576.1:c.364-86_364-74delinsGCTTCCCCAGTGT	ENSP00000496101.1:n.364-86_364-74delinsGCTTCCCCAGTGT
ENST00000646664.1:c.364-38_364-26delinsGCTTCCCCAGTGT MANE Select	ENSP00000494750.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000647275.1:c.-3-38_-3-26delinsGCTTCCCCAGTGT	ENSP00000494185.1:n.-3-38_-3-26delinsGCTTCCCCAGTGT
ENST00000674681.1:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000502821.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000675515.1:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000501862.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000676189.1:c.375-50_375-38delinsGCTTCCCCAGTGT	ENSP00000502538.1:n.375-50_375-38delinsGCTTCCCCAGTGT
ENST00000676319.1:c.87+814_87+826delinsGCTTCCCCAGTGT	ENSP00000502193.1:n.87+814_87+826delinsGCTTCCCCAGTGT
ENST00000676397.1:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000502286.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000331789.9:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000349960.4:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000425660.5:c.*27-38_*27-26delinsGCTTCCCCAGTGT	ENSP00000409264.1:n.*27-38_*27-26delinsGCTTCCCCAGTGT
ENST00000432588.5:c.364-38_364-26delinsGCTTCCCCAGTGT	ENSP00000407473.1:n.364-38_364-26delinsGCTTCCCCAGTGT
ENST00000462494.5:n.851_863delinsGCTTCCCCAGTGT
ENST00000473257.1:n.82-38_82-26delinsGCTTCCCCAGTGT
ENST00000477812.1:n.571-38_571-26delinsGCTTCCCCAGTGT
ENST00000484841.5:n.519-38_519-26delinsGCTTCCCCAGTGT
ENST00000493945.5:n.370-38_370-26delinsGCTTCCCCAGTGT
NM_001101.3:c.364-38_364-26delinsGCTTCCCCAGTGT , LRG_132t1:c.364-38_364-26delinsGCTTCCCCAGTGT	NP_001092.1:n.364-38_364-26delinsGCTTCCCCAGTGT
XM_006715764.1:c.-41_-29delinsGCTTCCCCAGTGT	XP_006715827.1:n.-41_-29delinsGCTTCCCCAGTGT
NM_001101.4:c.364-38_364-26delinsGCTTCCCCAGTGT	NP_001092.1:n.364-38_364-26delinsGCTTCCCCAGTGT
NM_001101.5:c.364-38_364-26delinsGCTTCCCCAGTGT MANE Select	NP_001092.1:n.364-38_364-26delinsGCTTCCCCAGTGT