Canonical Allele Identifier: CA2681650000

Gene: ACTB

Linked Data

• gnomAD v4: 7-5529508-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529509del , CM000669.2:g.5529509del	GRCh38
NC_000007.13:g.5569140del , CM000669.1:g.5569140del	GRCh37
NC_000007.12:g.5535666del	NCBI36
NG_007992.1:g.6093del , LRG_132:g.6093del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.123+26del	ENSP00000399487.2:n.123+26del
ENST00000432588.6:c.123+26del	ENSP00000407473.2:n.123+26del
ENST00000473257.3:c.-6-109del	ENSP00000501773.1:n.-6-109del
ENST00000477812.2:n.222del
ENST00000484841.6:n.277+26del
ENST00000493945.6:c.123+26del	ENSP00000494269.1:n.123+26del
ENST00000642480.2:c.123+26del	ENSP00000495995.2:n.123+26del
ENST00000645025.1:n.206+26del
ENST00000645576.1:c.123+26del	ENSP00000496101.1:n.123+26del
ENST00000646664.1:c.123+26del MANE Select	ENSP00000494750.1:n.123+26del
ENST00000647275.1:c.-3-790del	ENSP00000494185.1:n.-3-790del
ENST00000674681.1:c.123+26del	ENSP00000502821.1:n.123+26del
ENST00000675515.1:c.123+26del	ENSP00000501862.1:n.123+26del
ENST00000676189.1:c.123+26del	ENSP00000502538.1:n.123+26del
ENST00000676319.1:c.87+62del	ENSP00000502193.1:n.87+62del
ENST00000676397.1:c.123+26del	ENSP00000502286.1:n.123+26del
ENST00000331789.9:c.123+26del	ENSP00000349960.4:n.123+26del
ENST00000414620.1:c.123+26del	ENSP00000401032.1:n.123+26del
ENST00000417101.1:c.132+26del	ENSP00000399487.1:n.132+26del
ENST00000425660.5:c.123+26del	ENSP00000409264.1:n.123+26del
ENST00000432588.5:c.123+26del	ENSP00000407473.1:n.123+26del
ENST00000443528.5:c.123+26del	ENSP00000393951.1:n.123+26del
ENST00000462494.5:n.207+26del
ENST00000473257.1:n.82-790del
ENST00000477812.1:n.222del
ENST00000480301.1:n.215del
ENST00000484841.5:n.278+26del
ENST00000493945.5:n.129+26del
NM_001101.3:c.123+26del , LRG_132t1:c.123+26del	NP_001092.1:n.123+26del
NM_001101.4:c.123+26del	NP_001092.1:n.123+26del
NM_001101.5:c.123+26del MANE Select	NP_001092.1:n.123+26del