Canonical Allele Identifier: CA726642148
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs1251811623

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18124295_18124296del , CM000679.2:g.18124295_18124296del GRCh38
NC_000017.10:g.18027609_18027610del , CM000679.1:g.18027609_18027610del GRCh37
NC_000017.9:g.17968334_17968335del NCBI36
NG_011634.1:g.20590_20591del
NG_011634.2:g.20590_20591del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.3610-188_3610-187del MANE Select ENSP00000495481.1:n.3610-188_3610-187del
ENST00000651088.1:c.151-188_151-187del ENSP00000498988.1:n.151-188_151-187del
ENST00000205890.9:c.3610-188_3610-187del ENSP00000205890.5:n.3610-188_3610-187del
ENST00000583079.1:n.5128_5129del
ENST00000615845.4:c.3610-188_3610-187del ENSP00000481642.1:n.3610-188_3610-187del
NM_016239.3:c.3610-188_3610-187del NP_057323.3:n.3610-188_3610-187del
XM_011523917.1:c.3610-188_3610-187del XP_011522219.1:n.3610-188_3610-187del
XM_011523918.1:c.3610-188_3610-187del XP_011522220.1:n.3610-188_3610-187del
XM_011523919.1:c.3610-188_3610-187del XP_011522221.1:n.3610-188_3610-187del
XM_011523920.1:c.3610-188_3610-187del XP_011522222.1:n.3610-188_3610-187del
XM_011523921.1:c.3610-188_3610-187del XP_011522223.1:n.3610-188_3610-187del
XR_934037.1:n.4269-188_4269-187del
XR_934038.1:n.4269-188_4269-187del
XR_934039.1:n.4269-188_4269-187del
XM_011523918.2:c.3610-188_3610-187del XP_011522220.1:n.3610-188_3610-187del
XM_017024714.2:c.3610-188_3610-187del XP_016880203.1:n.3610-188_3610-187del
XM_017024715.2:c.3610-188_3610-187del XP_016880204.1:n.3610-188_3610-187del
XM_024450780.1:c.3610-188_3610-187del XP_024306548.1:n.3610-188_3610-187del
XM_024450781.1:c.3610-188_3610-187del XP_024306549.1:n.3610-188_3610-187del
XM_024450782.1:c.3610-188_3610-187del XP_024306550.1:n.3610-188_3610-187del
XR_934039.2:n.4308-188_4308-187del
NM_016239.4:c.3610-188_3610-187del MANE Select NP_057323.3:n.3610-188_3610-187del