Canonical Allele Identifier: CA2574087899

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636602del , CM000663.2:g.171636602del GRCh38
NC_000001.10:g.171605742del , CM000663.1:g.171605742del GRCh37
NC_000001.9:g.169872365del NCBI36
NG_008859.1:g.21032del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.838del (MYOC) MANE Select ENSP00000037502.5:p.Tyr280ThrfsTer?
ENST00000637303.1:c.235-2028del (MYOCOS) ENSP00000490048.1:n.235-2028del
ENST00000638471.1:c.*176del (MYOC) ENSP00000491206.1:n.*176del
ENST00000037502.10:c.838del (MYOC) ENSP00000037502.5:p.Tyr280ThrfsTer?
ENST00000614688.1:c.838del (MYOC) ENSP00000478680.1:p.Tyr280ThrfsTer?
NM_000261.1:c.838del (MYOC) NP_000252.1:p.Tyr280ThrfsTer?
NM_000261.2:c.838del (MYOC) MANE Select NP_000252.1:p.Tyr280ThrfsTer?