Canonical Allele Identifier: CA2649105843

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635633del , CM000663.2:g.171635633del GRCh38
NC_000001.10:g.171604773del , CM000663.1:g.171604773del GRCh37
NC_000001.9:g.169871396del NCBI36
NG_008859.1:g.22002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*293del (MYOC) MANE Select ENSP00000037502.5:n.*293del
ENST00000637303.1:c.235-2997del (MYOCOS) ENSP00000490048.1:n.235-2997del
ENST00000638471.1:c.*1146del (MYOC) ENSP00000491206.1:n.*1146del
ENST00000037502.10:c.*293del (MYOC) ENSP00000037502.5:n.*293del
ENST00000614688.1:c.*772del (MYOC) ENSP00000478680.1:n.*772del
NM_000261.1:c.*293del (MYOC) NP_000252.1:n.*293del
NM_000261.2:c.*293del (MYOC) MANE Select NP_000252.1:n.*293del