Canonical Allele Identifier: CA2681649987

Gene: ACTB

Linked Data

• gnomAD v4: 7-5529483-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529483C>A , CM000669.2:g.5529483C>A	GRCh38
NC_000007.13:g.5569114C>A , CM000669.1:g.5569114C>A	GRCh37
NC_000007.12:g.5535640C>A	NCBI36
NG_007992.1:g.6119G>T , LRG_132:g.6119G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.123+52G>T	ENSP00000399487.2:n.123+52G>T
ENST00000432588.6:c.123+52G>T	ENSP00000407473.2:n.123+52G>T
ENST00000473257.3:c.-6-83G>T	ENSP00000501773.1:n.-6-83G>T
ENST00000477812.2:n.248G>T
ENST00000484841.6:n.277+52G>T
ENST00000493945.6:c.123+52G>T	ENSP00000494269.1:n.123+52G>T
ENST00000642480.2:c.123+52G>T	ENSP00000495995.2:n.123+52G>T
ENST00000645025.1:n.206+52G>T
ENST00000645576.1:c.123+52G>T	ENSP00000496101.1:n.123+52G>T
ENST00000646664.1:c.123+52G>T MANE Select	ENSP00000494750.1:n.123+52G>T
ENST00000647275.1:c.-3-764G>T	ENSP00000494185.1:n.-3-764G>T
ENST00000674681.1:c.123+52G>T	ENSP00000502821.1:n.123+52G>T
ENST00000675515.1:c.123+52G>T	ENSP00000501862.1:n.123+52G>T
ENST00000676189.1:c.123+52G>T	ENSP00000502538.1:n.123+52G>T
ENST00000676319.1:c.87+88G>T	ENSP00000502193.1:n.87+88G>T
ENST00000676397.1:c.123+52G>T	ENSP00000502286.1:n.123+52G>T
ENST00000331789.9:c.123+52G>T	ENSP00000349960.4:n.123+52G>T
ENST00000414620.1:c.123+52G>T	ENSP00000401032.1:n.123+52G>T
ENST00000417101.1:c.132+52G>T	ENSP00000399487.1:n.132+52G>T
ENST00000425660.5:c.123+52G>T	ENSP00000409264.1:n.123+52G>T
ENST00000432588.5:c.123+52G>T	ENSP00000407473.1:n.123+52G>T
ENST00000443528.5:c.123+52G>T	ENSP00000393951.1:n.123+52G>T
ENST00000462494.5:n.207+52G>T
ENST00000473257.1:n.82-764G>T
ENST00000477812.1:n.248G>T
ENST00000480301.1:n.241G>T
ENST00000484841.5:n.278+52G>T
ENST00000493945.5:n.129+52G>T
NM_001101.3:c.123+52G>T , LRG_132t1:c.123+52G>T	NP_001092.1:n.123+52G>T
NM_001101.4:c.123+52G>T	NP_001092.1:n.123+52G>T
NM_001101.5:c.123+52G>T MANE Select	NP_001092.1:n.123+52G>T