Canonical Allele Identifier: CA394869142
Gene: MYH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.15750286C>G , CM000678.2:g.15750286C>G GRCh38
NC_000016.9:g.15844143C>G , CM000678.1:g.15844143C>G GRCh37
NC_000016.8:g.15751644C>G NCBI36
NG_009299.1:g.111745G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300036.6:c.1910G>C MANE Select ENSP00000300036.5:p.Ser637Thr
ENST00000452625.7:c.1931G>C MANE Plus Clinical ENSP00000407821.2:p.Ser644Thr
ENST00000576790.7:c.1910G>C ENSP00000458731.1:p.Ser637Thr
ENST00000652121.1:c.*93G>C ENSP00000498314.1:n.*93G>C
ENST00000300036.5:c.1910G>C ENSP00000300036.5:p.Ser637Thr
ENST00000396324.7:c.1931G>C ENSP00000379616.3:p.Ser644Thr
ENST00000452625.6:c.1931G>C ENSP00000407821.2:p.Ser644Thr
ENST00000570785.1:n.2332G>C
ENST00000576790.6:c.1910G>C ENSP00000458731.1:p.Ser637Thr
ENST00000616439.4:c.1931G>C ENSP00000484924.1:p.Ser644Thr
NM_001040113.1:c.1931G>C NP_001035202.1:p.Ser644Thr
NM_001040114.1:c.1931G>C NP_001035203.1:p.Ser644Thr
NM_002474.2:c.1910G>C NP_002465.1:p.Ser637Thr
NM_022844.2:c.1910G>C NP_074035.1:p.Ser637Thr
XM_011522502.1:c.1910G>C XP_011520804.1:p.Ser637Thr
XM_011522502.2:c.1910G>C XP_011520804.1:p.Ser637Thr
XM_017023250.1:c.1931G>C XP_016878739.1:p.Ser644Thr
NM_002474.3:c.1910G>C MANE Select NP_002465.1:p.Ser637Thr
NM_001040113.2:c.1931G>C MANE Plus Clinical NP_001035202.1:p.Ser644Thr
NM_001040114.2:c.1931G>C NP_001035203.1:p.Ser644Thr
NM_022844.3:c.1910G>C NP_074035.1:p.Ser637Thr