Canonical Allele Identifier: CA2746620467

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636742_171636743del , CM000663.2:g.171636742_171636743del GRCh38
NC_000001.10:g.171605882_171605883del , CM000663.1:g.171605882_171605883del GRCh37
NC_000001.9:g.169872505_169872506del NCBI36
NG_008859.1:g.20891_20892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-34_731-33del (MYOC) MANE Select ENSP00000037502.5:n.731-34_731-33del
ENST00000637303.1:c.235-1888_235-1887del (MYOCOS) ENSP00000490048.1:n.235-1888_235-1887del
ENST00000638471.1:c.*69-34_*69-33del (MYOC) ENSP00000491206.1:n.*69-34_*69-33del
ENST00000037502.10:c.731-34_731-33del (MYOC) ENSP00000037502.5:n.731-34_731-33del
ENST00000614688.1:c.731-34_731-33del (MYOC) ENSP00000478680.1:n.731-34_731-33del
NM_000261.1:c.731-34_731-33del (MYOC) NP_000252.1:n.731-34_731-33del
NM_000261.2:c.731-34_731-33del (MYOC) MANE Select NP_000252.1:n.731-34_731-33del