Canonical Allele Identifier: CA2681649659

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528725-A-ATCTTCTCGCGGTTGGCCTTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528725_5528726insTCTTCTCGCGGTTGGCCTTGG , CM000669.2:g.5528725_5528726insTCTTCTCGCGGTTGGCCTTGG	GRCh38
NC_000007.13:g.5568356_5568357insTCTTCTCGCGGTTGGCCTTGG , CM000669.1:g.5568356_5568357insTCTTCTCGCGGTTGGCCTTGG	GRCh37
NC_000007.12:g.5534882_5534883insTCTTCTCGCGGTTGGCCTTGG	NCBI36
NG_007992.1:g.6876_6877insCCAAGGCCAACCGCGAGAAGA , LRG_132:g.6876_6877insCCAAGGCCAACCGCGAGAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000407473.2:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000473257.3:c.235-7_235-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000501773.1:n.235-7_235-6insCCAAGGCCAACCGCGAGAAGA
ENST00000477812.2:n.904_905insCCAAGGCCAACCGCGAGAAGA
ENST00000484841.6:n.559-7_559-6insCCAAGGCCAACCGCGAGAAGA
ENST00000493945.6:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000494269.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000642480.2:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000495995.2:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000645576.1:c.364-55_364-54insCCAAGGCCAACCGCGAGAAGA	ENSP00000496101.1:n.364-55_364-54insCCAAGGCCAACCGCGAGAAGA
ENST00000646664.1:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA MANE Select	ENSP00000494750.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000647275.1:c.-3-7_-3-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000494185.1:n.-3-7_-3-6insCCAAGGCCAACCGCGAGAAGA
ENST00000674681.1:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000502821.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000675515.1:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000501862.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000676189.1:c.375-19_375-18insCCAAGGCCAACCGCGAGAAGA	ENSP00000502538.1:n.375-19_375-18insCCAAGGCCAACCGCGAGAAGA
ENST00000676319.1:c.87+845_87+846insCCAAGGCCAACCGCGAGAAGA	ENSP00000502193.1:n.87+845_87+846insCCAAGGCCAACCGCGAGAAGA
ENST00000676397.1:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000502286.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000331789.9:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000349960.4:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000425660.5:c.*27-7_*27-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000409264.1:n.*27-7_*27-6insCCAAGGCCAACCGCGAGAAGA
ENST00000432588.5:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	ENSP00000407473.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
ENST00000462494.5:n.882_883insCCAAGGCCAACCGCGAGAAGA
ENST00000473257.1:n.82-7_82-6insCCAAGGCCAACCGCGAGAAGA
ENST00000477812.1:n.571-7_571-6insCCAAGGCCAACCGCGAGAAGA
ENST00000484841.5:n.519-7_519-6insCCAAGGCCAACCGCGAGAAGA
ENST00000493945.5:n.370-7_370-6insCCAAGGCCAACCGCGAGAAGA
NM_001101.3:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA , LRG_132t1:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	NP_001092.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
XM_006715764.1:c.-10_-9insCCAAGGCCAACCGCGAGAAGA	XP_006715827.1:n.-10_-9insCCAAGGCCAACCGCGAGAAGA
NM_001101.4:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA	NP_001092.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA
NM_001101.5:c.364-7_364-6insCCAAGGCCAACCGCGAGAAGA MANE Select	NP_001092.1:n.364-7_364-6insCCAAGGCCAACCGCGAGAAGA