Canonical Allele Identifier: CA1684987988

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528399G= , CM000669.2:g.5528399G=	GRCh38
NC_000007.13:g.5568030G= , CM000669.1:g.5568030G=	GRCh37
NC_000007.12:g.5534556G=	NCBI36
NG_007992.1:g.7203C= , LRG_132:g.7203C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.684C=	ENSP00000407473.2:p.Ala228=
ENST00000473257.3:c.555C=	ENSP00000501773.1:p.Ala185=
ENST00000477812.2:n.1231C=
ENST00000493945.6:c.684C=	ENSP00000494269.1:p.Ala228=
ENST00000642480.2:c.684C=	ENSP00000495995.2:p.Ala228=
ENST00000645576.1:c.636C=	ENSP00000496101.1:p.Ala212=
ENST00000646664.1:c.684C= MANE Select	ENSP00000494750.1:p.Ala228=
ENST00000647275.1:c.318C=	ENSP00000494185.1:p.Ala106=
ENST00000674681.1:c.684C=	ENSP00000502821.1:p.Ala228=
ENST00000675515.1:c.684C=	ENSP00000501862.1:p.Ala228=
ENST00000676189.1:c.*227C=	ENSP00000502538.1:n.*227C=
ENST00000676319.1:c.88-616C=	ENSP00000502193.1:n.88-616C=
ENST00000676397.1:c.684C=	ENSP00000502286.1:p.Ala228=
ENST00000331789.9:c.684C=	ENSP00000349960.4:p.Ala228=
ENST00000425660.5:c.*347C=	ENSP00000409264.1:n.*347C=
ENST00000462494.5:n.1209C=
ENST00000473257.1:n.402C=
ENST00000484841.5:n.839C=
ENST00000493945.5:n.690C=
NM_001101.3:c.684C= , LRG_132t1:c.684C=	NP_001092.1:p.Ala228=
XM_006715764.1:c.318C=	XP_006715827.1:p.Ala106=
NM_001101.4:c.684C=	NP_001092.1:p.Ala228=
NM_001101.5:c.684C= MANE Select	NP_001092.1:p.Ala228=