Canonical Allele Identifier: CA453639159

Gene: ACTB

Linked Data

• gnomAD v4: 7-5528504-G-A
• MyVariant Identifiers: chr7:g.5568135G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528504G>A , CM000669.2:g.5528504G>A	GRCh38
NC_000007.13:g.5568135G>A , CM000669.1:g.5568135G>A	GRCh37
NC_000007.12:g.5534661G>A	NCBI36
NG_007992.1:g.7098C>T , LRG_132:g.7098C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.579C>T	ENSP00000407473.2:p.Leu193=
ENST00000473257.3:c.450C>T	ENSP00000501773.1:p.Leu150=
ENST00000477812.2:n.1126C>T
ENST00000493945.6:c.579C>T	ENSP00000494269.1:p.Leu193=
ENST00000642480.2:c.579C>T	ENSP00000495995.2:p.Leu193=
ENST00000645576.1:c.531C>T	ENSP00000496101.1:p.Leu177=
ENST00000646664.1:c.579C>T MANE Select	ENSP00000494750.1:p.Leu193=
ENST00000647275.1:c.213C>T	ENSP00000494185.1:p.Leu71=
ENST00000674681.1:c.579C>T	ENSP00000502821.1:p.Leu193=
ENST00000675515.1:c.579C>T	ENSP00000501862.1:p.Leu193=
ENST00000676189.1:c.*122C>T	ENSP00000502538.1:n.*122C>T
ENST00000676319.1:c.88-721C>T	ENSP00000502193.1:n.88-721C>T
ENST00000676397.1:c.579C>T	ENSP00000502286.1:p.Leu193=
ENST00000331789.9:c.579C>T	ENSP00000349960.4:p.Leu193=
ENST00000425660.5:c.*242C>T	ENSP00000409264.1:n.*242C>T
ENST00000462494.5:n.1104C>T
ENST00000473257.1:n.297C>T
ENST00000477812.1:n.786C>T
ENST00000484841.5:n.734C>T
ENST00000493945.5:n.585C>T
NM_001101.3:c.579C>T , LRG_132t1:c.579C>T	NP_001092.1:p.Leu193=
XM_006715764.1:c.213C>T	XP_006715827.1:p.Leu71=
NM_001101.4:c.579C>T	NP_001092.1:p.Leu193=
NM_001101.5:c.579C>T MANE Select	NP_001092.1:p.Leu193=