Canonical Allele Identifier: CA1207016670

Linked Data

dbSNP Id: rs1558085561

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635873dup , CM000663.2:g.171635873dup GRCh38
NC_000001.10:g.171605013dup , CM000663.1:g.171605013dup GRCh37
NC_000001.9:g.169871636dup NCBI36
NG_008859.1:g.21766dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*57dup (MYOC) MANE Select ENSP00000037502.5:n.*57dup
ENST00000637303.1:c.235-2757dup (MYOCOS) ENSP00000490048.1:n.235-2757dup
ENST00000638471.1:c.*910dup (MYOC) ENSP00000491206.1:n.*910dup
ENST00000037502.10:c.*57dup (MYOC) ENSP00000037502.5:n.*57dup
ENST00000614688.1:c.*536dup (MYOC) ENSP00000478680.1:n.*536dup
NM_000261.1:c.*57dup (MYOC) NP_000252.1:n.*57dup
NM_000261.2:c.*57dup (MYOC) MANE Select NP_000252.1:n.*57dup