Canonical Allele Identifier: CA2649106560
Gene: MYOC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171651916dup , CM000663.2:g.171651916dup GRCh38
NC_000001.10:g.171621056dup , CM000663.1:g.171621056dup GRCh37
NC_000001.9:g.169887679dup NCBI36
NG_008859.1:g.5720dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.604+94dup MANE Select ENSP00000037502.5:n.604+94dup
ENST00000638471.1:c.130+568dup ENSP00000491206.1:n.130+568dup
ENST00000037502.10:c.604+94dup ENSP00000037502.5:n.604+94dup
ENST00000614688.1:c.604+94dup ENSP00000478680.1:n.604+94dup
NM_000261.1:c.604+94dup NP_000252.1:n.604+94dup
NM_000261.2:c.604+94dup MANE Select NP_000252.1:n.604+94dup