Canonical Allele Identifier: CA2209945590

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15778752A= , CM000678.2:g.15778752A=	GRCh38
NC_000016.9:g.15872609A= , CM000678.1:g.15872609A=	GRCh37
NC_000016.8:g.15780110A=	NCBI36
NG_009299.1:g.83279T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.790+28T= MANE Select	ENSP00000300036.5:n.790+28T=
ENST00000452625.7:c.811+28T= MANE Plus Clinical	ENSP00000407821.2:n.811+28T=
ENST00000571910.2:n.174+28T=
ENST00000576790.7:c.790+28T=	ENSP00000458731.1:n.790+28T=
ENST00000652121.1:c.790+28T=	ENSP00000498314.1:n.790+28T=
ENST00000300036.5:c.790+28T=	ENSP00000300036.5:n.790+28T=
ENST00000396324.7:c.811+28T=	ENSP00000379616.3:n.811+28T=
ENST00000452625.6:c.811+28T=	ENSP00000407821.2:n.811+28T=
ENST00000570785.1:n.1212+28T=
ENST00000571910.1:n.644+28T=
ENST00000576790.6:c.790+28T=	ENSP00000458731.1:n.790+28T=
ENST00000616439.4:c.811+28T=	ENSP00000484924.1:n.811+28T=
NM_001040113.1:c.811+28T=	NP_001035202.1:n.811+28T=
NM_001040114.1:c.811+28T=	NP_001035203.1:n.811+28T=
NM_002474.2:c.790+28T=	NP_002465.1:n.790+28T=
NM_022844.2:c.790+28T=	NP_074035.1:n.790+28T=
XM_011522502.1:c.790+28T=	XP_011520804.1:n.790+28T=
XM_011522502.2:c.790+28T=	XP_011520804.1:n.790+28T=
XM_017023250.1:c.811+28T=	XP_016878739.1:n.811+28T=
NM_002474.3:c.790+28T= MANE Select	NP_002465.1:n.790+28T=
NM_001040113.2:c.811+28T= MANE Plus Clinical	NP_001035202.1:n.811+28T=
NM_001040114.2:c.811+28T=	NP_001035203.1:n.811+28T=
NM_022844.3:c.790+28T=	NP_074035.1:n.790+28T=