Canonical Allele Identifier: CA1207023181
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652253_171652254delinsTC , CM000663.2:g.171652253_171652254delinsTC GRCh38
NC_000001.10:g.171621393_171621394delinsTC , CM000663.1:g.171621393_171621394delinsTC GRCh37
NC_000001.9:g.169888016_169888017delinsTC NCBI36
NG_008859.1:g.5380_5381delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.358_359delinsGA MANE Select ENSP00000037502.5:p.Glu120=
ENST00000638471.1:c.130+228_130+229delinsGA ENSP00000491206.1:n.130+228_130+229delinsGA
ENST00000037502.10:c.358_359delinsGA ENSP00000037502.5:p.Glu120=
ENST00000614688.1:c.358_359delinsGA ENSP00000478680.1:p.Glu120=
NM_000261.1:c.358_359delinsGA NP_000252.1:p.Glu120=
NM_000261.2:c.358_359delinsGA MANE Select NP_000252.1:p.Glu120=