Canonical Allele Identifier: CA1148420620
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652546_171652547delinsAA , CM000663.2:g.171652546_171652547delinsAA GRCh38
NC_000001.10:g.171621686_171621687delinsAA , CM000663.1:g.171621686_171621687delinsAA GRCh37
NC_000001.9:g.169888309_169888310delinsAA NCBI36
NG_008859.1:g.5087_5088delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.65_66delinsTT MANE Select ENSP00000037502.5:p.Leu22=
ENST00000638471.1:c.65_66delinsTT ENSP00000491206.1:p.Leu22=
ENST00000037502.10:c.65_66delinsTT ENSP00000037502.5:p.Leu22=
ENST00000614688.1:c.65_66delinsTT ENSP00000478680.1:p.Leu22=
NM_000261.1:c.65_66delinsTT NP_000252.1:p.Leu22=
NM_000261.2:c.65_66delinsTT MANE Select NP_000252.1:p.Leu22=