Canonical Allele Identifier: CA2209930388
Gene: MYH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.15750126G= , CM000678.2:g.15750126G= GRCh38
NC_000016.9:g.15843983G= , CM000678.1:g.15843983G= GRCh37
NC_000016.8:g.15751484G= NCBI36
NG_009299.1:g.111905C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300036.6:c.2058+12C= MANE Select ENSP00000300036.5:n.2058+12C=
ENST00000452625.7:c.2079+12C= MANE Plus Clinical ENSP00000407821.2:n.2079+12C=
ENST00000576790.7:c.2058+12C= ENSP00000458731.1:n.2058+12C=
ENST00000652121.1:c.*241+12C= ENSP00000498314.1:n.*241+12C=
ENST00000300036.5:c.2058+12C= ENSP00000300036.5:n.2058+12C=
ENST00000396324.7:c.2079+12C= ENSP00000379616.3:n.2079+12C=
ENST00000452625.6:c.2079+12C= ENSP00000407821.2:n.2079+12C=
ENST00000570785.1:n.2492C=
ENST00000576790.6:c.2058+12C= ENSP00000458731.1:n.2058+12C=
ENST00000616439.4:c.2079+12C= ENSP00000484924.1:n.2079+12C=
NM_001040113.1:c.2079+12C= NP_001035202.1:n.2079+12C=
NM_001040114.1:c.2079+12C= NP_001035203.1:n.2079+12C=
NM_002474.2:c.2058+12C= NP_002465.1:n.2058+12C=
NM_022844.2:c.2058+12C= NP_074035.1:n.2058+12C=
XM_011522502.1:c.2058+12C= XP_011520804.1:n.2058+12C=
XM_011522502.2:c.2058+12C= XP_011520804.1:n.2058+12C=
XM_017023250.1:c.2079+12C= XP_016878739.1:n.2079+12C=
NM_002474.3:c.2058+12C= MANE Select NP_002465.1:n.2058+12C=
NM_001040113.2:c.2079+12C= MANE Plus Clinical NP_001035202.1:n.2079+12C=
NM_001040114.2:c.2079+12C= NP_001035203.1:n.2079+12C=
NM_022844.3:c.2058+12C= NP_074035.1:n.2058+12C=