Canonical Allele Identifier: CA2746620459

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636735_171636736del , CM000663.2:g.171636735_171636736del GRCh38
NC_000001.10:g.171605875_171605876del , CM000663.1:g.171605875_171605876del GRCh37
NC_000001.9:g.169872498_169872499del NCBI36
NG_008859.1:g.20898_20899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-27_731-26del (MYOC) MANE Select ENSP00000037502.5:n.731-27_731-26del
ENST00000637303.1:c.235-1895_235-1894del (MYOCOS) ENSP00000490048.1:n.235-1895_235-1894del
ENST00000638471.1:c.*69-27_*69-26del (MYOC) ENSP00000491206.1:n.*69-27_*69-26del
ENST00000037502.10:c.731-27_731-26del (MYOC) ENSP00000037502.5:n.731-27_731-26del
ENST00000614688.1:c.731-27_731-26del (MYOC) ENSP00000478680.1:n.731-27_731-26del
NM_000261.1:c.731-27_731-26del (MYOC) NP_000252.1:n.731-27_731-26del
NM_000261.2:c.731-27_731-26del (MYOC) MANE Select NP_000252.1:n.731-27_731-26del