Canonical Allele Identifier: CA2746620475

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636746_171636748del , CM000663.2:g.171636746_171636748del GRCh38
NC_000001.10:g.171605886_171605888del , CM000663.1:g.171605886_171605888del GRCh37
NC_000001.9:g.169872509_169872511del NCBI36
NG_008859.1:g.20886_20888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-39_731-37del (MYOC) MANE Select ENSP00000037502.5:n.731-39_731-37del
ENST00000637303.1:c.235-1884_235-1882del (MYOCOS) ENSP00000490048.1:n.235-1884_235-1882del
ENST00000638471.1:c.*69-39_*69-37del (MYOC) ENSP00000491206.1:n.*69-39_*69-37del
ENST00000037502.10:c.731-39_731-37del (MYOC) ENSP00000037502.5:n.731-39_731-37del
ENST00000614688.1:c.731-39_731-37del (MYOC) ENSP00000478680.1:n.731-39_731-37del
NM_000261.1:c.731-39_731-37del (MYOC) NP_000252.1:n.731-39_731-37del
NM_000261.2:c.731-39_731-37del (MYOC) MANE Select NP_000252.1:n.731-39_731-37del