Canonical Allele Identifier: CA453639220

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568264G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528633G>T , CM000669.2:g.5528633G>T	GRCh38
NC_000007.13:g.5568264G>T , CM000669.1:g.5568264G>T	GRCh37
NC_000007.12:g.5534790G>T	NCBI36
NG_007992.1:g.6969C>A , LRG_132:g.6969C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.450C>A	ENSP00000407473.2:p.Gly150=
ENST00000473257.3:c.321C>A	ENSP00000501773.1:p.Gly107=
ENST00000477812.2:n.997C>A
ENST00000493945.6:c.450C>A	ENSP00000494269.1:p.Gly150=
ENST00000642480.2:c.450C>A	ENSP00000495995.2:p.Gly150=
ENST00000645576.1:c.402C>A	ENSP00000496101.1:p.Gly134=
ENST00000646664.1:c.450C>A MANE Select	ENSP00000494750.1:p.Gly150=
ENST00000647275.1:c.84C>A	ENSP00000494185.1:p.Gly28=
ENST00000674681.1:c.450C>A	ENSP00000502821.1:p.Gly150=
ENST00000675515.1:c.450C>A	ENSP00000501862.1:p.Gly150=
ENST00000676189.1:c.449C>A	ENSP00000502538.1:p.Ala150Glu
ENST00000676319.1:c.88-850C>A	ENSP00000502193.1:n.88-850C>A
ENST00000676397.1:c.450C>A	ENSP00000502286.1:p.Gly150=
ENST00000331789.9:c.450C>A	ENSP00000349960.4:p.Gly150=
ENST00000425660.5:c.*113C>A	ENSP00000409264.1:n.*113C>A
ENST00000432588.5:c.450C>A	ENSP00000407473.1:p.Gly150=
ENST00000462494.5:n.975C>A
ENST00000473257.1:n.168C>A
ENST00000477812.1:n.657C>A
ENST00000484841.5:n.605C>A
ENST00000493945.5:n.456C>A
NM_001101.3:c.450C>A , LRG_132t1:c.450C>A	NP_001092.1:p.Gly150=
XM_006715764.1:c.84C>A	XP_006715827.1:p.Gly28=
NM_001101.4:c.450C>A	NP_001092.1:p.Gly150=
NM_001101.5:c.450C>A MANE Select	NP_001092.1:p.Gly150=