Canonical Allele Identifier: CA2636459806
Community Standard Title: NM_016239.4(MYO15A):c.10572del (p.Ser3525AlafsTer29)
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18178849del , CM000679.2:g.18178849del GRCh38
NC_000017.10:g.18082163del , CM000679.1:g.18082163del GRCh37
NC_000017.9:g.18022888del NCBI36
NG_011634.1:g.75144del
NG_011634.2:g.75144del

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.10572del MANE Select NP_057323.3:p.Ser3525AlafsTer29
ENST00000647165.2:c.10572del MANE Select ENSP00000495481.1:p.Ser3525AlafsTer29
NM_016239.3:c.10572del NP_057323.3:p.Ser3525AlafsTer29
ENST00000205890.9:c.10572del ENSP00000205890.5:p.Ser3525AlafsTer29
ENST00000418233.7:c.*22del ENSP00000408800.3:n.*22del
ENST00000433411.7:n.2098del
ENST00000578575.1:c.1025del
ENST00000579848.6:c.903del ENSP00000465910.1:n.903del
ENST00000615845.4:c.10572del ENSP00000481642.1:p.Ser3525AlafsTer29
ENST00000642418.1:n.3052del
ENST00000643693.1:n.2514del
ENST00000644795.1:c.*22del ENSP00000495720.1:n.*22del
ENST00000646782.1:n.3568del
ENST00000651214.1:n.3055del
XM_011523921.1:c.10566del XP_011522223.1:p.Ser3523AlafsTer29
XM_017024714.2:c.10512del XP_016880203.1:p.Ser3505AlafsTer29
XM_017024715.2:c.10575del XP_016880204.1:p.Ser3526AlafsTer29