Canonical Allele Identifier: CA2649106607
Gene: MYOC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652397_171652399del , CM000663.2:g.171652397_171652399del GRCh38
NC_000001.10:g.171621537_171621539del , CM000663.1:g.171621537_171621539del GRCh37
NC_000001.9:g.169888160_169888162del NCBI36
NG_008859.1:g.5235_5237del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.213_215del MANE Select ENSP00000037502.5:p.His72del
ENST00000638471.1:c.130+83_130+85del ENSP00000491206.1:n.130+83_130+85del
ENST00000037502.10:c.213_215del ENSP00000037502.5:p.His72del
ENST00000614688.1:c.213_215del ENSP00000478680.1:p.His72del
NM_000261.1:c.213_215del NP_000252.1:p.His72del
NM_000261.2:c.213_215del MANE Select NP_000252.1:p.His72del