Canonical Allele Identifier: CA1684977594

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529531_5529532delinsCT , CM000669.2:g.5529531_5529532delinsCT	GRCh38
NC_000007.13:g.5569162_5569163delinsCT , CM000669.1:g.5569162_5569163delinsCT	GRCh37
NC_000007.12:g.5535688_5535689delinsCT	NCBI36
NG_007992.1:g.6070_6071delinsAG , LRG_132:g.6070_6071delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.123+3_123+4delinsAG	ENSP00000399487.2:n.123+3_123+4delinsAG
ENST00000432588.6:c.123+3_123+4delinsAG	ENSP00000407473.2:n.123+3_123+4delinsAG
ENST00000473257.3:c.-6-132_-6-131delinsAG	ENSP00000501773.1:n.-6-132_-6-131delinsAG
ENST00000477812.2:n.199_200delinsAG
ENST00000484841.6:n.277+3_277+4delinsAG
ENST00000493945.6:c.123+3_123+4delinsAG	ENSP00000494269.1:n.123+3_123+4delinsAG
ENST00000642480.2:c.123+3_123+4delinsAG	ENSP00000495995.2:n.123+3_123+4delinsAG
ENST00000645025.1:n.206+3_206+4delinsAG
ENST00000645576.1:c.123+3_123+4delinsAG	ENSP00000496101.1:n.123+3_123+4delinsAG
ENST00000646664.1:c.123+3_123+4delinsAG MANE Select	ENSP00000494750.1:n.123+3_123+4delinsAG
ENST00000647275.1:c.-3-813_-3-812delinsAG	ENSP00000494185.1:n.-3-813_-3-812delinsAG
ENST00000674681.1:c.123+3_123+4delinsAG	ENSP00000502821.1:n.123+3_123+4delinsAG
ENST00000675515.1:c.123+3_123+4delinsAG	ENSP00000501862.1:n.123+3_123+4delinsAG
ENST00000676189.1:c.123+3_123+4delinsAG	ENSP00000502538.1:n.123+3_123+4delinsAG
ENST00000676319.1:c.87+39_87+40delinsAG	ENSP00000502193.1:n.87+39_87+40delinsAG
ENST00000676397.1:c.123+3_123+4delinsAG	ENSP00000502286.1:n.123+3_123+4delinsAG
ENST00000331789.9:c.123+3_123+4delinsAG	ENSP00000349960.4:n.123+3_123+4delinsAG
ENST00000414620.1:c.123+3_123+4delinsAG	ENSP00000401032.1:n.123+3_123+4delinsAG
ENST00000417101.1:c.132+3_132+4delinsAG	ENSP00000399487.1:n.132+3_132+4delinsAG
ENST00000425660.5:c.123+3_123+4delinsAG	ENSP00000409264.1:n.123+3_123+4delinsAG
ENST00000432588.5:c.123+3_123+4delinsAG	ENSP00000407473.1:n.123+3_123+4delinsAG
ENST00000443528.5:c.123+3_123+4delinsAG	ENSP00000393951.1:n.123+3_123+4delinsAG
ENST00000462494.5:n.207+3_207+4delinsAG
ENST00000473257.1:n.82-813_82-812delinsAG
ENST00000477812.1:n.199_200delinsAG
ENST00000480301.1:n.192_193delinsAG
ENST00000484841.5:n.278+3_278+4delinsAG
ENST00000493945.5:n.129+3_129+4delinsAG
NM_001101.3:c.123+3_123+4delinsAG , LRG_132t1:c.123+3_123+4delinsAG	NP_001092.1:n.123+3_123+4delinsAG
NM_001101.4:c.123+3_123+4delinsAG	NP_001092.1:n.123+3_123+4delinsAG
NM_001101.5:c.123+3_123+4delinsAG MANE Select	NP_001092.1:n.123+3_123+4delinsAG