Canonical Allele Identifier: CA2649105992

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635942_171635952del , CM000663.2:g.171635942_171635952del GRCh38
NC_000001.10:g.171605082_171605092del , CM000663.1:g.171605082_171605092del GRCh37
NC_000001.9:g.169871705_169871715del NCBI36
NG_008859.1:g.21682_21692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1488_1498del (MYOC) MANE Select ENSP00000037502.5:p.Tyr497AlafsTer?
ENST00000637303.1:c.235-2688_235-2678del (MYOCOS) ENSP00000490048.1:n.235-2688_235-2678del
ENST00000638471.1:c.*826_*836del (MYOC) ENSP00000491206.1:n.*826_*836del
ENST00000037502.10:c.1488_1498del (MYOC) ENSP00000037502.5:p.Tyr497AlafsTer?
ENST00000614688.1:c.*452_*462del (MYOC) ENSP00000478680.1:n.*452_*462del
NM_000261.1:c.1488_1498del (MYOC) NP_000252.1:p.Tyr497AlafsTer?
NM_000261.2:c.1488_1498del (MYOC) MANE Select NP_000252.1:p.Tyr497AlafsTer?