Canonical Allele Identifier: CA2839218435
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18138193del , CM000679.2:g.18138193del GRCh38
NC_000017.10:g.18041507del , CM000679.1:g.18041507del GRCh37
NC_000017.9:g.17982232del NCBI36
NG_011634.1:g.34488del
NG_011634.2:g.34488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646238.1:n.218del
ENST00000647165.2:c.4954del MANE Select ENSP00000495481.1:p.Leu1652Ter
ENST00000205890.9:c.4954del ENSP00000205890.5:p.Leu1652Ter
ENST00000615845.4:c.4954del ENSP00000481642.1:p.Leu1652Ter
NM_016239.3:c.4954del NP_057323.3:p.Leu1652Ter
XM_011523917.1:c.4948del XP_011522219.1:p.Leu1650Ter
XM_011523918.1:c.4948del XP_011522220.1:p.Leu1650Ter
XM_011523919.1:c.4948del XP_011522221.1:p.Leu1650Ter
XM_011523920.1:c.4948del XP_011522222.1:p.Leu1650Ter
XM_011523921.1:c.4948del XP_011522223.1:p.Leu1650Ter
XR_934037.1:n.5607del
XR_934038.1:n.5607del
XR_934039.1:n.5607del
XM_011523918.2:c.4948del XP_011522220.1:p.Leu1650Ter
XM_017024714.2:c.4948del XP_016880203.1:p.Leu1650Ter
XM_017024715.2:c.4957del XP_016880204.1:p.Leu1653Ter
XM_024450780.1:c.4948del XP_024306548.1:p.Leu1650Ter
XM_024450781.1:c.4948del XP_024306549.1:p.Leu1650Ter
XM_024450782.1:c.4948del XP_024306550.1:p.Leu1650Ter
XR_934039.2:n.5646del
NM_016239.4:c.4954del MANE Select NP_057323.3:p.Leu1652Ter