Canonical Allele Identifier: CA2649106602
Gene: MYOC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652360del , CM000663.2:g.171652360del GRCh38
NC_000001.10:g.171621500del , CM000663.1:g.171621500del GRCh37
NC_000001.9:g.169888123del NCBI36
NG_008859.1:g.5275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.253del MANE Select ENSP00000037502.5:p.Leu85TrpfsTer18
ENST00000638471.1:c.130+123del ENSP00000491206.1:n.130+123del
ENST00000037502.10:c.253del ENSP00000037502.5:p.Leu85TrpfsTer18
ENST00000614688.1:c.253del ENSP00000478680.1:p.Leu85TrpfsTer18
NM_000261.1:c.253del NP_000252.1:p.Leu85TrpfsTer18
NM_000261.2:c.253del MANE Select NP_000252.1:p.Leu85TrpfsTer18