Canonical Allele Identifier: CA2250782782
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18124294_18124296delinsCAT , CM000679.2:g.18124294_18124296delinsCAT GRCh38
NC_000017.10:g.18027608_18027610delinsCAT , CM000679.1:g.18027608_18027610delinsCAT GRCh37
NC_000017.9:g.17968333_17968335delinsCAT NCBI36
NG_011634.1:g.20589_20591delinsCAT
NG_011634.2:g.20589_20591delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.3610-189_3610-187delinsCAT MANE Select ENSP00000495481.1:n.3610-189_3610-187delinsCAT
ENST00000651088.1:c.151-189_151-187delinsCAT ENSP00000498988.1:n.151-189_151-187delinsCAT
ENST00000205890.9:c.3610-189_3610-187delinsCAT ENSP00000205890.5:n.3610-189_3610-187delinsCAT
ENST00000583079.1:n.5127_5129delinsCAT
ENST00000615845.4:c.3610-189_3610-187delinsCAT ENSP00000481642.1:n.3610-189_3610-187delinsCAT
NM_016239.3:c.3610-189_3610-187delinsCAT NP_057323.3:n.3610-189_3610-187delinsCAT
XM_011523917.1:c.3610-189_3610-187delinsCAT XP_011522219.1:n.3610-189_3610-187delinsCAT
XM_011523918.1:c.3610-189_3610-187delinsCAT XP_011522220.1:n.3610-189_3610-187delinsCAT
XM_011523919.1:c.3610-189_3610-187delinsCAT XP_011522221.1:n.3610-189_3610-187delinsCAT
XM_011523920.1:c.3610-189_3610-187delinsCAT XP_011522222.1:n.3610-189_3610-187delinsCAT
XM_011523921.1:c.3610-189_3610-187delinsCAT XP_011522223.1:n.3610-189_3610-187delinsCAT
XR_934037.1:n.4269-189_4269-187delinsCAT
XR_934038.1:n.4269-189_4269-187delinsCAT
XR_934039.1:n.4269-189_4269-187delinsCAT
XM_011523918.2:c.3610-189_3610-187delinsCAT XP_011522220.1:n.3610-189_3610-187delinsCAT
XM_017024714.2:c.3610-189_3610-187delinsCAT XP_016880203.1:n.3610-189_3610-187delinsCAT
XM_017024715.2:c.3610-189_3610-187delinsCAT XP_016880204.1:n.3610-189_3610-187delinsCAT
XM_024450780.1:c.3610-189_3610-187delinsCAT XP_024306548.1:n.3610-189_3610-187delinsCAT
XM_024450781.1:c.3610-189_3610-187delinsCAT XP_024306549.1:n.3610-189_3610-187delinsCAT
XM_024450782.1:c.3610-189_3610-187delinsCAT XP_024306550.1:n.3610-189_3610-187delinsCAT
XR_934039.2:n.4308-189_4308-187delinsCAT
NM_016239.4:c.3610-189_3610-187delinsCAT MANE Select NP_057323.3:n.3610-189_3610-187delinsCAT