Canonical Allele Identifier: CA2649105949

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635835del , CM000663.2:g.171635835del GRCh38
NC_000001.10:g.171604975del , CM000663.1:g.171604975del GRCh37
NC_000001.9:g.169871598del NCBI36
NG_008859.1:g.21801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*92del (MYOC) MANE Select ENSP00000037502.5:n.*92del
ENST00000637303.1:c.235-2795del (MYOCOS) ENSP00000490048.1:n.235-2795del
ENST00000638471.1:c.*945del (MYOC) ENSP00000491206.1:n.*945del
ENST00000037502.10:c.*92del (MYOC) ENSP00000037502.5:n.*92del
ENST00000614688.1:c.*571del (MYOC) ENSP00000478680.1:n.*571del
NM_000261.1:c.*92del (MYOC) NP_000252.1:n.*92del
NM_000261.2:c.*92del (MYOC) MANE Select NP_000252.1:n.*92del