Canonical Allele Identifier: CA2209930378
Gene: MYH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.15750114_15750117delinsCAGG , CM000678.2:g.15750114_15750117delinsCAGG GRCh38
NC_000016.9:g.15843971_15843974delinsCAGG , CM000678.1:g.15843971_15843974delinsCAGG GRCh37
NC_000016.8:g.15751472_15751475delinsCAGG NCBI36
NG_009299.1:g.111914_111917delinsCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000300036.6:c.2058+21_2058+24delinsCCTG MANE Select ENSP00000300036.5:n.2058+21_2058+24delins...
ENST00000452625.7:c.2079+21_2079+24delinsCCTG MANE Plus Clinical ENSP00000407821.2:n.2079+21_2079+24delins...
ENST00000576790.7:c.2058+21_2058+24delinsCCTG ENSP00000458731.1:n.2058+21_2058+24delins...
ENST00000652121.1:c.*241+21_*241+24delinsCCTG ENSP00000498314.1:n.*241+21_*241+24delins...
ENST00000300036.5:c.2058+21_2058+24delinsCCTG ENSP00000300036.5:n.2058+21_2058+24delins...
ENST00000396324.7:c.2079+21_2079+24delinsCCTG ENSP00000379616.3:n.2079+21_2079+24delins...
ENST00000452625.6:c.2079+21_2079+24delinsCCTG ENSP00000407821.2:n.2079+21_2079+24delins...
ENST00000570785.1:n.2501_2504delinsCCTG
ENST00000576790.6:c.2058+21_2058+24delinsCCTG ENSP00000458731.1:n.2058+21_2058+24delins...
ENST00000616439.4:c.2079+21_2079+24delinsCCTG ENSP00000484924.1:n.2079+21_2079+24delins...
NM_001040113.1:c.2079+21_2079+24delinsCCTG NP_001035202.1:n.2079+21_2079+24delinsCCT...
NM_001040114.1:c.2079+21_2079+24delinsCCTG NP_001035203.1:n.2079+21_2079+24delinsCCT...
NM_002474.2:c.2058+21_2058+24delinsCCTG NP_002465.1:n.2058+21_2058+24delinsCCTG
NM_022844.2:c.2058+21_2058+24delinsCCTG NP_074035.1:n.2058+21_2058+24delinsCCTG
XM_011522502.1:c.2058+21_2058+24delinsCCTG XP_011520804.1:n.2058+21_2058+24delinsCCT...
XM_011522502.2:c.2058+21_2058+24delinsCCTG XP_011520804.1:n.2058+21_2058+24delinsCCT...
XM_017023250.1:c.2079+21_2079+24delinsCCTG XP_016878739.1:n.2079+21_2079+24delinsCCT...
NM_002474.3:c.2058+21_2058+24delinsCCTG MANE Select NP_002465.1:n.2058+21_2058+24delinsCCTG
NM_001040113.2:c.2079+21_2079+24delinsCCTG MANE Plus Clinical NP_001035202.1:n.2079+21_2079+24delinsCCT...
NM_001040114.2:c.2079+21_2079+24delinsCCTG NP_001035203.1:n.2079+21_2079+24delinsCCT...
NM_022844.3:c.2058+21_2058+24delinsCCTG NP_074035.1:n.2058+21_2058+24delinsCCTG