Canonical Allele Identifier: CA1684976452

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528982_5528988delinsCAGAAAA , CM000669.2:g.5528982_5528988delinsCAGAAAA	GRCh38
NC_000007.13:g.5568613_5568619delinsCAGAAAA , CM000669.1:g.5568613_5568619delinsCAGAAAA	GRCh37
NC_000007.12:g.5535139_5535145delinsCAGAAAA	NCBI36
NG_007992.1:g.6614_6620delinsTTTTCTG , LRG_132:g.6614_6620delinsTTTTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+173_363+179delinsTTTTCTG	ENSP00000407473.2:n.363+173_363+179delinsTTTTCTG
ENST00000473257.3:c.234+173_234+179delinsTTTTCTG	ENSP00000501773.1:n.234+173_234+179delinsTTTTCTG
ENST00000477812.2:n.642_648delinsTTTTCTG
ENST00000484841.6:n.558+31_558+37delinsTTTTCTG
ENST00000493945.6:c.363+173_363+179delinsTTTTCTG	ENSP00000494269.1:n.363+173_363+179delinsTTTTCTG
ENST00000642480.2:c.363+173_363+179delinsTTTTCTG	ENSP00000495995.2:n.363+173_363+179delinsTTTTCTG
ENST00000645025.1:n.518_524delinsTTTTCTG
ENST00000645576.1:c.363+173_363+179delinsTTTTCTG	ENSP00000496101.1:n.363+173_363+179delinsTTTTCTG
ENST00000646664.1:c.363+173_363+179delinsTTTTCTG MANE Select	ENSP00000494750.1:n.363+173_363+179delinsTTTTCTG
ENST00000647275.1:c.-3-269_-3-263delinsTTTTCTG	ENSP00000494185.1:n.-3-269_-3-263delinsTTTTCTG
ENST00000674681.1:c.363+173_363+179delinsTTTTCTG	ENSP00000502821.1:n.363+173_363+179delinsTTTTCTG
ENST00000675515.1:c.363+173_363+179delinsTTTTCTG	ENSP00000501862.1:n.363+173_363+179delinsTTTTCTG
ENST00000676189.1:c.374+162_374+168delinsTTTTCTG	ENSP00000502538.1:n.374+162_374+168delinsTTTTCTG
ENST00000676319.1:c.87+583_87+589delinsTTTTCTG	ENSP00000502193.1:n.87+583_87+589delinsTTTTCTG
ENST00000676397.1:c.363+173_363+179delinsTTTTCTG	ENSP00000502286.1:n.363+173_363+179delinsTTTTCTG
ENST00000331789.9:c.363+173_363+179delinsTTTTCTG	ENSP00000349960.4:n.363+173_363+179delinsTTTTCTG
ENST00000425660.5:c.*26+31_*26+37delinsTTTTCTG	ENSP00000409264.1:n.*26+31_*26+37delinsTTTTCTG
ENST00000432588.5:c.363+173_363+179delinsTTTTCTG	ENSP00000407473.1:n.363+173_363+179delinsTTTTCTG
ENST00000462494.5:n.620_626delinsTTTTCTG
ENST00000473257.1:n.82-269_82-263delinsTTTTCTG
ENST00000477812.1:n.570+173_570+179delinsTTTTCTG
ENST00000484841.5:n.518+173_518+179delinsTTTTCTG
ENST00000493945.5:n.369+173_369+179delinsTTTTCTG
NM_001101.3:c.363+173_363+179delinsTTTTCTG , LRG_132t1:c.363+173_363+179delinsTTTTCTG	NP_001092.1:n.363+173_363+179delinsTTTTCTG
XM_006715764.1:c.-272_-266delinsTTTTCTG	XP_006715827.1:n.-272_-266delinsTTTTCTG
NM_001101.4:c.363+173_363+179delinsTTTTCTG	NP_001092.1:n.363+173_363+179delinsTTTTCTG
NM_001101.5:c.363+173_363+179delinsTTTTCTG MANE Select	NP_001092.1:n.363+173_363+179delinsTTTTCTG