Canonical Allele Identifier: CA1261181381

Gene: ACTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914847A= , CM000664.2:g.73914847A=	GRCh38
NC_000002.11:g.74141974A= , CM000664.1:g.74141974A=	GRCh37
NC_000002.10:g.73995482A=	NCBI36
NG_034140.1:g.26882A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.781A= MANE Select	ENSP00000295137.3:p.Thr261=
ENST00000345517.7:c.781A=	ENSP00000295137.3:p.Thr261=
ENST00000409624.1:c.781A=	ENSP00000386857.1:p.Thr261=
ENST00000409731.7:c.652A=	ENSP00000386929.3:p.Thr218=
ENST00000438902.6:c.*846A=	ENSP00000410706.2:n.*846A=
NM_001199893.1:c.652A=	NP_001186822.1:p.Thr218=
NM_001615.3:c.781A=	NP_001606.1:p.Thr261=
NM_001199893.2:c.652A=	NP_001186822.1:p.Thr218=
NM_001615.4:c.781A= MANE Select	NP_001606.1:p.Thr261=