Canonical Allele Identifier: CA2681649796

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528884-GGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528885_5528886del , CM000669.2:g.5528885_5528886del	GRCh38
NC_000007.13:g.5568516_5568517del , CM000669.1:g.5568516_5568517del	GRCh37
NC_000007.12:g.5535042_5535043del	NCBI36
NG_007992.1:g.6716_6717del , LRG_132:g.6716_6717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-167_364-166del	ENSP00000407473.2:n.364-167_364-166del
ENST00000473257.3:c.235-167_235-166del	ENSP00000501773.1:n.235-167_235-166del
ENST00000477812.2:n.744_745del
ENST00000484841.6:n.558+133_558+134del
ENST00000493945.6:c.364-167_364-166del	ENSP00000494269.1:n.364-167_364-166del
ENST00000642480.2:c.364-167_364-166del	ENSP00000495995.2:n.364-167_364-166del
ENST00000645576.1:c.364-215_364-214del	ENSP00000496101.1:n.364-215_364-214del
ENST00000646664.1:c.364-167_364-166del MANE Select	ENSP00000494750.1:n.364-167_364-166del
ENST00000647275.1:c.-3-167_-3-166del	ENSP00000494185.1:n.-3-167_-3-166del
ENST00000674681.1:c.364-167_364-166del	ENSP00000502821.1:n.364-167_364-166del
ENST00000675515.1:c.364-167_364-166del	ENSP00000501862.1:n.364-167_364-166del
ENST00000676189.1:c.375-179_375-178del	ENSP00000502538.1:n.375-179_375-178del
ENST00000676319.1:c.87+685_87+686del	ENSP00000502193.1:n.87+685_87+686del
ENST00000676397.1:c.364-167_364-166del	ENSP00000502286.1:n.364-167_364-166del
ENST00000331789.9:c.364-167_364-166del	ENSP00000349960.4:n.364-167_364-166del
ENST00000425660.5:c.*26+133_*26+134del	ENSP00000409264.1:n.*26+133_*26+134del
ENST00000432588.5:c.364-167_364-166del	ENSP00000407473.1:n.364-167_364-166del
ENST00000462494.5:n.722_723del
ENST00000473257.1:n.82-167_82-166del
ENST00000477812.1:n.571-167_571-166del
ENST00000484841.5:n.519-167_519-166del
ENST00000493945.5:n.370-167_370-166del
NM_001101.3:c.364-167_364-166del , LRG_132t1:c.364-167_364-166del	NP_001092.1:n.364-167_364-166del
XM_006715764.1:c.-170_-169del	XP_006715827.1:n.-170_-169del
NM_001101.4:c.364-167_364-166del	NP_001092.1:n.364-167_364-166del
NM_001101.5:c.364-167_364-166del MANE Select	NP_001092.1:n.364-167_364-166del