Canonical Allele Identifier: CA2746628357
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652660_171652664del , CM000663.2:g.171652660_171652664del GRCh38
NC_000001.10:g.171621800_171621804del , CM000663.1:g.171621800_171621804del GRCh37
NC_000001.9:g.169888423_169888427del NCBI36
NG_008859.1:g.4970_4974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-53_-49del MANE Select ENSP00000037502.5:n.-53_-49del
ENST00000037502.10:c.-53_-49del ENSP00000037502.5:n.-53_-49del
NM_000261.2:c.-53_-49del MANE Select NP_000252.1:n.-53_-49del