Canonical Allele Identifier: CA1139655085

Linked Data

ClinVar Variation Id: 1342199
ClinVar RCV Id: RCV001838866
dbSNP Id: rs2102944704

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636432del , CM000663.2:g.171636432del GRCh38
NC_000001.10:g.171605572del , CM000663.1:g.171605572del GRCh37
NC_000001.9:g.169872195del NCBI36
NG_008859.1:g.21203del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1009del (MYOC) MANE Select ENSP00000037502.5:p.Gln337ArgfsTer9
ENST00000637303.1:c.235-2198del (MYOCOS) ENSP00000490048.1:n.235-2198del
ENST00000638471.1:c.*347del (MYOC) ENSP00000491206.1:n.*347del
ENST00000037502.10:c.1009del (MYOC) ENSP00000037502.5:p.Gln337ArgfsTer9
ENST00000614688.1:c.1009-1del (MYOC)
NM_000261.1:c.1009del (MYOC) NP_000252.1:p.Gln337ArgfsTer9
NM_000261.2:c.1009del (MYOC) MANE Select NP_000252.1:p.Gln337ArgfsTer9