Canonical Allele Identifier: CA1207023150
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652185_171652189delinsTGTAG , CM000663.2:g.171652185_171652189delinsTGTAG GRCh38
NC_000001.10:g.171621325_171621329delinsTGTAG , CM000663.1:g.171621325_171621329delinsTGTAG GRCh37
NC_000001.9:g.169887948_169887952delinsTGTAG NCBI36
NG_008859.1:g.5445_5449delinsCTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.423_427delinsCTACA MANE Select ENSP00000037502.5:p.Ala141=
ENST00000638471.1:c.130+293_130+297delinsCTACA ENSP00000491206.1:n.130+293_130+297delinsCTACA
ENST00000037502.10:c.423_427delinsCTACA ENSP00000037502.5:p.Ala141=
ENST00000614688.1:c.423_427delinsCTACA ENSP00000478680.1:p.Ala141=
NM_000261.1:c.423_427delinsCTACA NP_000252.1:p.Ala141=
NM_000261.2:c.423_427delinsCTACA MANE Select NP_000252.1:p.Ala141=