Canonical Allele Identifier: CA2209930394

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15750138C= , CM000678.2:g.15750138C=	GRCh38
NC_000016.9:g.15843995C= , CM000678.1:g.15843995C=	GRCh37
NC_000016.8:g.15751496C=	NCBI36
NG_009299.1:g.111893G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.2058G= MANE Select	ENSP00000300036.5:p.Arg686=
ENST00000452625.7:c.2079G= MANE Plus Clinical	ENSP00000407821.2:p.Arg693=
ENST00000576790.7:c.2058G=	ENSP00000458731.1:p.Arg686=
ENST00000652121.1:c.*241G=	ENSP00000498314.1:n.*241G=
ENST00000300036.5:c.2058G=	ENSP00000300036.5:p.Arg686=
ENST00000396324.7:c.2079G=	ENSP00000379616.3:p.Arg693=
ENST00000452625.6:c.2079G=	ENSP00000407821.2:p.Arg693=
ENST00000570785.1:n.2480G=
ENST00000576790.6:c.2058G=	ENSP00000458731.1:p.Arg686=
ENST00000616439.4:c.2079G=	ENSP00000484924.1:p.Arg693=
NM_001040113.1:c.2079G=	NP_001035202.1:p.Arg693=
NM_001040114.1:c.2079G=	NP_001035203.1:p.Arg693=
NM_002474.2:c.2058G=	NP_002465.1:p.Arg686=
NM_022844.2:c.2058G=	NP_074035.1:p.Arg686=
XM_011522502.1:c.2058G=	XP_011520804.1:p.Arg686=
XM_011522502.2:c.2058G=	XP_011520804.1:p.Arg686=
XM_017023250.1:c.2079G=	XP_016878739.1:p.Arg693=
NM_002474.3:c.2058G= MANE Select	NP_002465.1:p.Arg686=
NM_001040113.2:c.2079G= MANE Plus Clinical	NP_001035202.1:p.Arg693=
NM_001040114.2:c.2079G=	NP_001035203.1:p.Arg693=
NM_022844.3:c.2058G=	NP_074035.1:p.Arg686=