Canonical Allele Identifier: CA366704516

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568885G>C (hg19) ; chr7:g.5529254G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529254G>C , CM000669.2:g.5529254G>C	GRCh38
NC_000007.13:g.5568885G>C , CM000669.1:g.5568885G>C	GRCh37
NC_000007.12:g.5535411G>C	NCBI36
NG_007992.1:g.6348C>G , LRG_132:g.6348C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.270C>G	ENSP00000399487.2:p.Phe90Leu
ENST00000432588.6:c.270C>G	ENSP00000407473.2:p.Phe90Leu
ENST00000473257.3:c.141C>G	ENSP00000501773.1:p.Phe47Leu
ENST00000477812.2:n.477C>G
ENST00000484841.6:n.424C>G
ENST00000493945.6:c.270C>G	ENSP00000494269.1:p.Phe90Leu
ENST00000642480.2:c.270C>G	ENSP00000495995.2:p.Phe90Leu
ENST00000645025.1:n.353C>G
ENST00000645576.1:c.270C>G	ENSP00000496101.1:p.Phe90Leu
ENST00000646664.1:c.270C>G MANE Select	ENSP00000494750.1:p.Phe90Leu
ENST00000647275.1:c.-3-535C>G	ENSP00000494185.1:n.-3-535C>G
ENST00000674681.1:c.270C>G	ENSP00000502821.1:p.Phe90Leu
ENST00000675515.1:c.270C>G	ENSP00000501862.1:p.Phe90Leu
ENST00000676189.1:c.270C>G	ENSP00000502538.1:p.Phe90Leu
ENST00000676319.1:c.87+317C>G	ENSP00000502193.1:n.87+317C>G
ENST00000676397.1:c.270C>G	ENSP00000502286.1:p.Phe90Leu
ENST00000331789.9:c.270C>G	ENSP00000349960.4:p.Phe90Leu
ENST00000417101.1:c.279C>G	ENSP00000399487.1:p.Phe93Leu
ENST00000425660.5:c.270C>G	ENSP00000409264.1:p.Phe90Leu
ENST00000432588.5:c.270C>G	ENSP00000407473.1:p.Phe90Leu
ENST00000443528.5:c.270C>G	ENSP00000393951.1:p.Phe90Leu
ENST00000462494.5:n.354C>G
ENST00000473257.1:n.82-535C>G
ENST00000477812.1:n.477C>G
ENST00000480301.1:n.470C>G
ENST00000484841.5:n.425C>G
ENST00000493945.5:n.276C>G
NM_001101.3:c.270C>G , LRG_132t1:c.270C>G	NP_001092.1:p.Phe90Leu
XM_006715764.1:c.-437C>G	XP_006715827.1:n.-437C>G
NM_001101.4:c.270C>G	NP_001092.1:p.Phe90Leu
NM_001101.5:c.270C>G MANE Select	NP_001092.1:p.Phe90Leu