Canonical Allele Identifier: CA2209945591

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15778754T= , CM000678.2:g.15778754T=	GRCh38
NC_000016.9:g.15872611T= , CM000678.1:g.15872611T=	GRCh37
NC_000016.8:g.15780112T=	NCBI36
NG_009299.1:g.83277A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300036.6:c.790+26A= MANE Select	ENSP00000300036.5:n.790+26A=
ENST00000452625.7:c.811+26A= MANE Plus Clinical	ENSP00000407821.2:n.811+26A=
ENST00000571910.2:n.174+26A=
ENST00000576790.7:c.790+26A=	ENSP00000458731.1:n.790+26A=
ENST00000652121.1:c.790+26A=	ENSP00000498314.1:n.790+26A=
ENST00000300036.5:c.790+26A=	ENSP00000300036.5:n.790+26A=
ENST00000396324.7:c.811+26A=	ENSP00000379616.3:n.811+26A=
ENST00000452625.6:c.811+26A=	ENSP00000407821.2:n.811+26A=
ENST00000570785.1:n.1212+26A=
ENST00000571910.1:n.644+26A=
ENST00000576790.6:c.790+26A=	ENSP00000458731.1:n.790+26A=
ENST00000616439.4:c.811+26A=	ENSP00000484924.1:n.811+26A=
NM_001040113.1:c.811+26A=	NP_001035202.1:n.811+26A=
NM_001040114.1:c.811+26A=	NP_001035203.1:n.811+26A=
NM_002474.2:c.790+26A=	NP_002465.1:n.790+26A=
NM_022844.2:c.790+26A=	NP_074035.1:n.790+26A=
XM_011522502.1:c.790+26A=	XP_011520804.1:n.790+26A=
XM_011522502.2:c.790+26A=	XP_011520804.1:n.790+26A=
XM_017023250.1:c.811+26A=	XP_016878739.1:n.811+26A=
NM_002474.3:c.790+26A= MANE Select	NP_002465.1:n.790+26A=
NM_001040113.2:c.811+26A= MANE Plus Clinical	NP_001035202.1:n.811+26A=
NM_001040114.2:c.811+26A=	NP_001035203.1:n.811+26A=
NM_022844.3:c.790+26A=	NP_074035.1:n.790+26A=