Canonical Allele Identifier: CA2649105993

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635957_171636008del , CM000663.2:g.171635957_171636008del GRCh38
NC_000001.10:g.171605097_171605148del , CM000663.1:g.171605097_171605148del GRCh37
NC_000001.9:g.169871720_169871771del NCBI36
NG_008859.1:g.21626_21677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1432_1483del (MYOC) MANE Select ENSP00000037502.5:p.Asp478SerfsTer?
ENST00000637303.1:c.235-2673_235-2622del (MYOCOS) ENSP00000490048.1:n.235-2673_235-2622del
ENST00000638471.1:c.*770_*821del (MYOC) ENSP00000491206.1:n.*770_*821del
ENST00000037502.10:c.1432_1483del (MYOC) ENSP00000037502.5:p.Asp478SerfsTer?
ENST00000614688.1:c.*396_*447del (MYOC) ENSP00000478680.1:n.*396_*447del
NM_000261.1:c.1432_1483del (MYOC) NP_000252.1:p.Asp478SerfsTer?
NM_000261.2:c.1432_1483del (MYOC) MANE Select NP_000252.1:p.Asp478SerfsTer?