Canonical Allele Identifier: CA1684977199

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529365A= , CM000669.2:g.5529365A=	GRCh38
NC_000007.13:g.5568996A= , CM000669.1:g.5568996A=	GRCh37
NC_000007.12:g.5535522A=	NCBI36
NG_007992.1:g.6237T= , LRG_132:g.6237T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.159T=	ENSP00000399487.2:p.Tyr53=
ENST00000432588.6:c.159T=	ENSP00000407473.2:p.Tyr53=
ENST00000473257.3:c.30T=	ENSP00000501773.1:p.Tyr10=
ENST00000477812.2:n.366T=
ENST00000484841.6:n.313T=
ENST00000493945.6:c.159T=	ENSP00000494269.1:p.Tyr53=
ENST00000642480.2:c.159T=	ENSP00000495995.2:p.Tyr53=
ENST00000645025.1:n.242T=
ENST00000645576.1:c.159T=	ENSP00000496101.1:p.Tyr53=
ENST00000646664.1:c.159T= MANE Select	ENSP00000494750.1:p.Tyr53=
ENST00000647275.1:c.-3-646T=	ENSP00000494185.1:n.-3-646T=
ENST00000674681.1:c.159T=	ENSP00000502821.1:p.Tyr53=
ENST00000675515.1:c.159T=	ENSP00000501862.1:p.Tyr53=
ENST00000676189.1:c.159T=	ENSP00000502538.1:p.Tyr53=
ENST00000676319.1:c.87+206T=	ENSP00000502193.1:n.87+206T=
ENST00000676397.1:c.159T=	ENSP00000502286.1:p.Tyr53=
ENST00000331789.9:c.159T=	ENSP00000349960.4:p.Tyr53=
ENST00000414620.1:c.159T=	ENSP00000401032.1:p.Tyr53=
ENST00000417101.1:c.168T=	ENSP00000399487.1:p.Tyr56=
ENST00000425660.5:c.159T=	ENSP00000409264.1:p.Tyr53=
ENST00000432588.5:c.159T=	ENSP00000407473.1:p.Tyr53=
ENST00000443528.5:c.159T=	ENSP00000393951.1:p.Tyr53=
ENST00000462494.5:n.243T=
ENST00000473257.1:n.82-646T=
ENST00000477812.1:n.366T=
ENST00000480301.1:n.359T=
ENST00000484841.5:n.314T=
ENST00000493945.5:n.165T=
NM_001101.3:c.159T= , LRG_132t1:c.159T=	NP_001092.1:p.Tyr53=
NM_001101.4:c.159T=	NP_001092.1:p.Tyr53=
NM_001101.5:c.159T= MANE Select	NP_001092.1:p.Tyr53=