Canonical Allele Identifier: CA2746620484

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636755_171636762del , CM000663.2:g.171636755_171636762del GRCh38
NC_000001.10:g.171605895_171605902del , CM000663.1:g.171605895_171605902del GRCh37
NC_000001.9:g.169872518_169872525del NCBI36
NG_008859.1:g.20872_20879del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-53_731-46del (MYOC) MANE Select ENSP00000037502.5:n.731-53_731-46del
ENST00000637303.1:c.235-1875_235-1868del (MYOCOS) ENSP00000490048.1:n.235-1875_235-1868del
ENST00000638471.1:c.*69-53_*69-46del (MYOC) ENSP00000491206.1:n.*69-53_*69-46del
ENST00000037502.10:c.731-53_731-46del (MYOC) ENSP00000037502.5:n.731-53_731-46del
ENST00000614688.1:c.731-53_731-46del (MYOC) ENSP00000478680.1:n.731-53_731-46del
NM_000261.1:c.731-53_731-46del (MYOC) NP_000252.1:n.731-53_731-46del
NM_000261.2:c.731-53_731-46del (MYOC) MANE Select NP_000252.1:n.731-53_731-46del