Canonical Allele Identifier: CA1684976358

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528942C= , CM000669.2:g.5528942C=	GRCh38
NC_000007.13:g.5568573C= , CM000669.1:g.5568573C=	GRCh37
NC_000007.12:g.5535099C=	NCBI36
NG_007992.1:g.6660G= , LRG_132:g.6660G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.363+219G=	ENSP00000407473.2:n.363+219G=
ENST00000473257.3:c.234+219G=	ENSP00000501773.1:n.234+219G=
ENST00000477812.2:n.688G=
ENST00000484841.6:n.558+77G=
ENST00000493945.6:c.363+219G=	ENSP00000494269.1:n.363+219G=
ENST00000642480.2:c.363+219G=	ENSP00000495995.2:n.363+219G=
ENST00000645025.1:n.564G=
ENST00000645576.1:c.363+219G=	ENSP00000496101.1:n.363+219G=
ENST00000646664.1:c.363+219G= MANE Select	ENSP00000494750.1:n.363+219G=
ENST00000647275.1:c.-3-223G=	ENSP00000494185.1:n.-3-223G=
ENST00000674681.1:c.363+219G=	ENSP00000502821.1:n.363+219G=
ENST00000675515.1:c.363+219G=	ENSP00000501862.1:n.363+219G=
ENST00000676189.1:c.374+208G=	ENSP00000502538.1:n.374+208G=
ENST00000676319.1:c.87+629G=	ENSP00000502193.1:n.87+629G=
ENST00000676397.1:c.363+219G=	ENSP00000502286.1:n.363+219G=
ENST00000331789.9:c.363+219G=	ENSP00000349960.4:n.363+219G=
ENST00000425660.5:c.*26+77G=	ENSP00000409264.1:n.*26+77G=
ENST00000432588.5:c.363+219G=	ENSP00000407473.1:n.363+219G=
ENST00000462494.5:n.666G=
ENST00000473257.1:n.82-223G=
ENST00000477812.1:n.570+219G=
ENST00000484841.5:n.518+219G=
ENST00000493945.5:n.369+219G=
NM_001101.3:c.363+219G= , LRG_132t1:c.363+219G=	NP_001092.1:n.363+219G=
XM_006715764.1:c.-226G=	XP_006715827.1:n.-226G=
NM_001101.4:c.363+219G=	NP_001092.1:n.363+219G=
NM_001101.5:c.363+219G= MANE Select	NP_001092.1:n.363+219G=