Canonical Allele Identifier: CA1261181380

Gene: ACTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914843T= , CM000664.2:g.73914843T=	GRCh38
NC_000002.11:g.74141970T= , CM000664.1:g.74141970T=	GRCh37
NC_000002.10:g.73995478T=	NCBI36
NG_034140.1:g.26878T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.777T= MANE Select	ENSP00000295137.3:p.Pro259=
ENST00000345517.7:c.777T=	ENSP00000295137.3:p.Pro259=
ENST00000409624.1:c.777T=	ENSP00000386857.1:p.Pro259=
ENST00000409731.7:c.648T=	ENSP00000386929.3:p.Pro216=
ENST00000438902.6:c.*842T=	ENSP00000410706.2:n.*842T=
NM_001199893.1:c.648T=	NP_001186822.1:p.Pro216=
NM_001615.3:c.777T=	NP_001606.1:p.Pro259=
NM_001199893.2:c.648T=	NP_001186822.1:p.Pro216=
NM_001615.4:c.777T= MANE Select	NP_001606.1:p.Pro259=