Canonical Allele Identifier: CA1261181383

Gene: ACTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914849C= , CM000664.2:g.73914849C=	GRCh38
NC_000002.11:g.74141976C= , CM000664.1:g.74141976C=	GRCh37
NC_000002.10:g.73995484C=	NCBI36
NG_034140.1:g.26884C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.783C= MANE Select	ENSP00000295137.3:p.Thr261=
ENST00000345517.7:c.783C=	ENSP00000295137.3:p.Thr261=
ENST00000409624.1:c.783C=	ENSP00000386857.1:p.Thr261=
ENST00000409731.7:c.654C=	ENSP00000386929.3:p.Thr218=
ENST00000438902.6:c.*848C=	ENSP00000410706.2:n.*848C=
NM_001199893.1:c.654C=	NP_001186822.1:p.Thr218=
NM_001615.3:c.783C=	NP_001606.1:p.Thr261=
NM_001199893.2:c.654C=	NP_001186822.1:p.Thr218=
NM_001615.4:c.783C= MANE Select	NP_001606.1:p.Thr261=