Canonical Allele Identifier: CA1261178770

Gene: ACTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73909130C= , CM000664.2:g.73909130C=	GRCh38
NC_000002.11:g.74136257C= , CM000664.1:g.74136257C=	GRCh37
NC_000002.10:g.73989765C=	NCBI36
NG_034140.1:g.21165C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001615.4:c.442C= MANE Select	NP_001606.1:p.Arg148=
ENST00000345517.8:c.442C= MANE Select	ENSP00000295137.3:p.Arg148=
NM_001199893.1:c.313C=	NP_001186822.1:p.Arg105=
NM_001199893.2:c.313C=	NP_001186822.1:p.Arg105=
NM_001615.3:c.442C=	NP_001606.1:p.Arg148=
ENST00000345517.7:c.442C=	ENSP00000295137.3:p.Arg148=
ENST00000409624.1:c.442C=	ENSP00000386857.1:p.Arg148=
ENST00000409731.7:c.313C=	ENSP00000386929.3:p.Arg105=
ENST00000429756.5:c.*197C=	ENSP00000392894.1:n.*197C=
ENST00000438902.6:c.*507C=	ENSP00000410706.2:n.*507C=