Canonical Allele Identifier: CA2746620451

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636714_171636818del , CM000663.2:g.171636714_171636818del GRCh38
NC_000001.10:g.171605854_171605958del , CM000663.1:g.171605854_171605958del GRCh37
NC_000001.9:g.169872477_169872581del NCBI36
NG_008859.1:g.20821_20925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-104_731del (MYOC)
ENST00000637303.1:c.235-1916_235-1812del (MYOCOS) ENSP00000490048.1:n.235-1916_235-1812del
ENST00000638471.1:c.*69-104_*69del (MYOC)
ENST00000037502.10:c.731-104_731del (MYOC)
ENST00000614688.1:c.731-104_731del (MYOC)
NM_000261.1:c.731-104_731del (MYOC)
NM_000261.2:c.731-104_731del (MYOC)