Canonical Allele Identifier: CA1009130224

Linked Data

dbSNP Id: rs1652906706

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635925del , CM000663.2:g.171635925del GRCh38
NC_000001.10:g.171605065del , CM000663.1:g.171605065del GRCh37
NC_000001.9:g.169871688del NCBI36
NG_008859.1:g.21712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*3del (MYOC) MANE Select ENSP00000037502.5:n.*3del
ENST00000637303.1:c.235-2705del (MYOCOS) ENSP00000490048.1:n.235-2705del
ENST00000638471.1:c.*856del (MYOC) ENSP00000491206.1:n.*856del
ENST00000037502.10:c.*3del (MYOC) ENSP00000037502.5:n.*3del
ENST00000614688.1:c.*482del (MYOC) ENSP00000478680.1:n.*482del
NM_000261.1:c.*3del (MYOC) NP_000252.1:n.*3del
NM_000261.2:c.*3del (MYOC) MANE Select NP_000252.1:n.*3del