Canonical Allele Identifier: CA1009116913
Gene: MYOC HGNC NCBI

Linked Data

dbSNP Id: rs1653369118

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652143del , CM000663.2:g.171652143del GRCh38
NC_000001.10:g.171621283del , CM000663.1:g.171621283del GRCh37
NC_000001.9:g.169887906del NCBI36
NG_008859.1:g.5492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.470del MANE Select ENSP00000037502.5:p.Lys157SerfsTer3
ENST00000638471.1:c.130+340del ENSP00000491206.1:n.130+340del
ENST00000037502.10:c.470del ENSP00000037502.5:p.Lys157SerfsTer3
ENST00000614688.1:c.470del ENSP00000478680.1:p.Lys157SerfsTer3
NM_000261.1:c.470del NP_000252.1:p.Lys157SerfsTer3
NM_000261.2:c.470del MANE Select NP_000252.1:p.Lys157SerfsTer3