Canonical Allele Identifier: CA2746620461

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636736_171636737del , CM000663.2:g.171636736_171636737del GRCh38
NC_000001.10:g.171605876_171605877del , CM000663.1:g.171605876_171605877del GRCh37
NC_000001.9:g.169872499_169872500del NCBI36
NG_008859.1:g.20897_20898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-28_731-27del (MYOC) MANE Select ENSP00000037502.5:n.731-28_731-27del
ENST00000637303.1:c.235-1894_235-1893del (MYOCOS) ENSP00000490048.1:n.235-1894_235-1893del
ENST00000638471.1:c.*69-28_*69-27del (MYOC) ENSP00000491206.1:n.*69-28_*69-27del
ENST00000037502.10:c.731-28_731-27del (MYOC) ENSP00000037502.5:n.731-28_731-27del
ENST00000614688.1:c.731-28_731-27del (MYOC) ENSP00000478680.1:n.731-28_731-27del
NM_000261.1:c.731-28_731-27del (MYOC) NP_000252.1:n.731-28_731-27del
NM_000261.2:c.731-28_731-27del (MYOC) MANE Select NP_000252.1:n.731-28_731-27del