Canonical Allele Identifier: CA2746628363
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652667_171652668insA , CM000663.2:g.171652667_171652668insA GRCh38
NC_000001.10:g.171621807_171621808insA , CM000663.1:g.171621807_171621808insA GRCh37
NC_000001.9:g.169888430_169888431insA NCBI36
NG_008859.1:g.4966_4967insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-57_-56insT MANE Select ENSP00000037502.5:n.-57_-56insT
ENST00000037502.10:c.-57_-56insT ENSP00000037502.5:n.-57_-56insT
NM_000261.2:c.-57_-56insT MANE Select NP_000252.1:n.-57_-56insT