Canonical Allele Identifier: CA2746628358
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652664_171652665insT , CM000663.2:g.171652664_171652665insT GRCh38
NC_000001.10:g.171621804_171621805insT , CM000663.1:g.171621804_171621805insT GRCh37
NC_000001.9:g.169888427_169888428insT NCBI36
NG_008859.1:g.4969_4970insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-54_-53insA MANE Select ENSP00000037502.5:n.-54_-53insA
ENST00000037502.10:c.-54_-53insA ENSP00000037502.5:n.-54_-53insA
NM_000261.2:c.-54_-53insA MANE Select NP_000252.1:n.-54_-53insA