Canonical Allele Identifier: CA2649105816

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635573del , CM000663.2:g.171635573del GRCh38
NC_000001.10:g.171604713del , CM000663.1:g.171604713del GRCh37
NC_000001.9:g.169871336del NCBI36
NG_008859.1:g.22065del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*356del (MYOC) MANE Select ENSP00000037502.5:n.*356del
ENST00000637303.1:c.235-3057del (MYOCOS) ENSP00000490048.1:n.235-3057del
ENST00000638471.1:c.*1209del (MYOC) ENSP00000491206.1:n.*1209del
ENST00000037502.10:c.*356del (MYOC) ENSP00000037502.5:n.*356del
ENST00000614688.1:c.*835del (MYOC) ENSP00000478680.1:n.*835del
NM_000261.1:c.*356del (MYOC) NP_000252.1:n.*356del
NM_000261.2:c.*356del (MYOC) MANE Select NP_000252.1:n.*356del