Canonical Allele Identifier: CA1261181376

Gene: ACTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914836G= , CM000664.2:g.73914836G=	GRCh38
NC_000002.11:g.74141963G= , CM000664.1:g.74141963G=	GRCh37
NC_000002.10:g.73995471G=	NCBI36
NG_034140.1:g.26871G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000345517.8:c.770G= MANE Select	ENSP00000295137.3:p.Arg257=
ENST00000345517.7:c.770G=	ENSP00000295137.3:p.Arg257=
ENST00000409624.1:c.770G=	ENSP00000386857.1:p.Arg257=
ENST00000409731.7:c.641G=	ENSP00000386929.3:p.Arg214=
ENST00000438902.6:c.*835G=	ENSP00000410706.2:n.*835G=
NM_001199893.1:c.641G=	NP_001186822.1:p.Arg214=
NM_001615.3:c.770G=	NP_001606.1:p.Arg257=
NM_001199893.2:c.641G=	NP_001186822.1:p.Arg214=
NM_001615.4:c.770G= MANE Select	NP_001606.1:p.Arg257=