Canonical Allele Identifier: CA2649106010

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636732_171636735dup , CM000663.2:g.171636732_171636735dup GRCh38
NC_000001.10:g.171605872_171605875dup , CM000663.1:g.171605872_171605875dup GRCh37
NC_000001.9:g.169872495_169872498dup NCBI36
NG_008859.1:g.20901_20904dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.731-24_731-21dup (MYOC) MANE Select ENSP00000037502.5:n.731-24_731-21dup
ENST00000637303.1:c.235-1898_235-1895dup (MYOCOS) ENSP00000490048.1:n.235-1898_235-1895dup
ENST00000638471.1:c.*69-24_*69-21dup (MYOC) ENSP00000491206.1:n.*69-24_*69-21dup
ENST00000037502.10:c.731-24_731-21dup (MYOC) ENSP00000037502.5:n.731-24_731-21dup
ENST00000614688.1:c.731-24_731-21dup (MYOC) ENSP00000478680.1:n.731-24_731-21dup
NM_000261.1:c.731-24_731-21dup (MYOC) NP_000252.1:n.731-24_731-21dup
NM_000261.2:c.731-24_731-21dup (MYOC) MANE Select NP_000252.1:n.731-24_731-21dup