Canonical Allele Identifier: CA2209930455

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15750288C= , CM000678.2:g.15750288C=	GRCh38
NC_000016.9:g.15844145C= , CM000678.1:g.15844145C=	GRCh37
NC_000016.8:g.15751646C=	NCBI36
NG_009299.1:g.111743G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.1908G= MANE Select	ENSP00000300036.5:p.Glu636=
ENST00000452625.7:c.1929G= MANE Plus Clinical	ENSP00000407821.2:p.Glu643=
ENST00000576790.7:c.1908G=	ENSP00000458731.1:p.Glu636=
ENST00000652121.1:c.*91G=	ENSP00000498314.1:n.*91G=
ENST00000300036.5:c.1908G=	ENSP00000300036.5:p.Glu636=
ENST00000396324.7:c.1929G=	ENSP00000379616.3:p.Glu643=
ENST00000452625.6:c.1929G=	ENSP00000407821.2:p.Glu643=
ENST00000570785.1:n.2330G=
ENST00000576790.6:c.1908G=	ENSP00000458731.1:p.Glu636=
ENST00000616439.4:c.1929G=	ENSP00000484924.1:p.Glu643=
NM_001040113.1:c.1929G=	NP_001035202.1:p.Glu643=
NM_001040114.1:c.1929G=	NP_001035203.1:p.Glu643=
NM_002474.2:c.1908G=	NP_002465.1:p.Glu636=
NM_022844.2:c.1908G=	NP_074035.1:p.Glu636=
XM_011522502.1:c.1908G=	XP_011520804.1:p.Glu636=
XM_011522502.2:c.1908G=	XP_011520804.1:p.Glu636=
XM_017023250.1:c.1929G=	XP_016878739.1:p.Glu643=
NM_002474.3:c.1908G= MANE Select	NP_002465.1:p.Glu636=
NM_001040113.2:c.1929G= MANE Plus Clinical	NP_001035202.1:p.Glu643=
NM_001040114.2:c.1929G=	NP_001035203.1:p.Glu643=
NM_022844.3:c.1908G=	NP_074035.1:p.Glu636=