Canonical Allele Identifier: CA1684988450

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528548C= , CM000669.2:g.5528548C=	GRCh38
NC_000007.13:g.5568179C= , CM000669.1:g.5568179C=	GRCh37
NC_000007.12:g.5534705C=	NCBI36
NG_007992.1:g.7054G= , LRG_132:g.7054G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.535G=	ENSP00000407473.2:p.Asp179=
ENST00000473257.3:c.406G=	ENSP00000501773.1:p.Asp136=
ENST00000477812.2:n.1082G=
ENST00000493945.6:c.535G=	ENSP00000494269.1:p.Asp179=
ENST00000642480.2:c.535G=	ENSP00000495995.2:p.Asp179=
ENST00000645576.1:c.487G=	ENSP00000496101.1:p.Asp163=
ENST00000646664.1:c.535G= MANE Select	ENSP00000494750.1:p.Asp179=
ENST00000647275.1:c.169G=	ENSP00000494185.1:p.Asp57=
ENST00000674681.1:c.535G=	ENSP00000502821.1:p.Asp179=
ENST00000675515.1:c.535G=	ENSP00000501862.1:p.Asp179=
ENST00000676189.1:c.*78G=	ENSP00000502538.1:n.*78G=
ENST00000676319.1:c.88-765G=	ENSP00000502193.1:n.88-765G=
ENST00000676397.1:c.535G=	ENSP00000502286.1:p.Asp179=
ENST00000331789.9:c.535G=	ENSP00000349960.4:p.Asp179=
ENST00000425660.5:c.*198G=	ENSP00000409264.1:n.*198G=
ENST00000462494.5:n.1060G=
ENST00000473257.1:n.253G=
ENST00000477812.1:n.742G=
ENST00000484841.5:n.690G=
ENST00000493945.5:n.541G=
NM_001101.3:c.535G= , LRG_132t1:c.535G=	NP_001092.1:p.Asp179=
XM_006715764.1:c.169G=	XP_006715827.1:p.Asp57=
NM_001101.4:c.535G=	NP_001092.1:p.Asp179=
NM_001101.5:c.535G= MANE Select	NP_001092.1:p.Asp179=