Canonical Allele Identifier: CA2746628348
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652636_171652637insACA , CM000663.2:g.171652636_171652637insACA GRCh38
NC_000001.10:g.171621776_171621777insACA , CM000663.1:g.171621776_171621777insACA GRCh37
NC_000001.9:g.169888399_169888400insACA NCBI36
NG_008859.1:g.4997_4998insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-26_-25insTGT MANE Select ENSP00000037502.5:n.-26_-25insTGT
ENST00000037502.10:c.-26_-25insTGT ENSP00000037502.5:n.-26_-25insTGT
NM_000261.2:c.-26_-25insTGT MANE Select NP_000252.1:n.-26_-25insTGT