Canonical Allele Identifier: CA1140503095

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635812_171635813delinsGG , CM000663.2:g.171635812_171635813delinsGG GRCh38
NC_000001.10:g.171604952_171604953delinsGG , CM000663.1:g.171604952_171604953delinsGG GRCh37
NC_000001.9:g.169871575_169871576delinsGG NCBI36
NG_008859.1:g.21821_21822delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*112_*113delinsCC (MYOC) MANE Select ENSP00000037502.5:n.*112_*113delinsCC
ENST00000637303.1:c.235-2818_235-2817delinsGG (MYOCOS) ENSP00000490048.1:n.235-2818_235-2817delinsGG
ENST00000638471.1:c.*965_*966delinsCC (MYOC) ENSP00000491206.1:n.*965_*966delinsCC
ENST00000037502.10:c.*112_*113delinsCC (MYOC) ENSP00000037502.5:n.*112_*113delinsCC
ENST00000614688.1:c.*591_*592delinsCC (MYOC) ENSP00000478680.1:n.*591_*592delinsCC
NM_000261.1:c.*112_*113delinsCC (MYOC) NP_000252.1:n.*112_*113delinsCC
NM_000261.2:c.*112_*113delinsCC (MYOC) MANE Select NP_000252.1:n.*112_*113delinsCC