Canonical Allele Identifier: CA2649105998

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636337_171636343dup , CM000663.2:g.171636337_171636343dup GRCh38
NC_000001.10:g.171605477_171605483dup , CM000663.1:g.171605477_171605483dup GRCh37
NC_000001.9:g.169872100_169872106dup NCBI36
NG_008859.1:g.21291_21297dup

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1097_1103dup (MYOC) MANE Select ENSP00000037502.5:p.Phe369ArgfsTer14
ENST00000637303.1:c.235-2293_235-2287dup (MYOCOS) ENSP00000490048.1:n.235-2293_235-2287dup
ENST00000638471.1:c.*435_*441dup (MYOC) ENSP00000491206.1:n.*435_*441dup
ENST00000037502.10:c.1097_1103dup (MYOC) ENSP00000037502.5:p.Phe369ArgfsTer14
ENST00000614688.1:c.*61_*67dup (MYOC) ENSP00000478680.1:n.*61_*67dup
NM_000261.1:c.1097_1103dup (MYOC) NP_000252.1:p.Phe369ArgfsTer14
NM_000261.2:c.1097_1103dup (MYOC) MANE Select NP_000252.1:p.Phe369ArgfsTer14