Canonical Allele Identifier: CA2649105997

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636190del , CM000663.2:g.171636190del GRCh38
NC_000001.10:g.171605330del , CM000663.1:g.171605330del GRCh37
NC_000001.9:g.169871953del NCBI36
NG_008859.1:g.21446del

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1252del (MYOC) MANE Select ENSP00000037502.5:p.Glu418ArgfsTer?
ENST00000637303.1:c.235-2440del (MYOCOS) ENSP00000490048.1:n.235-2440del
ENST00000638471.1:c.*590del (MYOC) ENSP00000491206.1:n.*590del
ENST00000037502.10:c.1252del (MYOC) ENSP00000037502.5:p.Glu418ArgfsTer?
ENST00000614688.1:c.*216del (MYOC) ENSP00000478680.1:n.*216del
NM_000261.1:c.1252del (MYOC) NP_000252.1:p.Glu418ArgfsTer?
NM_000261.2:c.1252del (MYOC) MANE Select NP_000252.1:p.Glu418ArgfsTer?