Canonical Allele Identifier: CA2636447441
Gene: MYO15A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145790_18145800del , CM000679.2:g.18145790_18145800del GRCh38
NC_000017.10:g.18049104_18049114del , CM000679.1:g.18049104_18049114del GRCh37
NC_000017.9:g.17989829_17989839del NCBI36
NG_011634.1:g.42085_42095del
NG_011634.2:g.42085_42095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-82_6274-72del MANE Select ENSP00000495481.1:n.6274-82_6274-72del
ENST00000205890.9:c.6274-82_6274-72del ENSP00000205890.5:n.6274-82_6274-72del
ENST00000615845.4:c.6274-82_6274-72del ENSP00000481642.1:n.6274-82_6274-72del
NM_016239.3:c.6274-82_6274-72del NP_057323.3:n.6274-82_6274-72del
XM_011523917.1:c.6214-82_6214-72del XP_011522219.1:n.6214-82_6214-72del
XM_011523918.1:c.6214-82_6214-72del XP_011522220.1:n.6214-82_6214-72del
XM_011523921.1:c.6268-82_6268-72del XP_011522223.1:n.6268-82_6268-72del
XR_934037.1:n.6873-82_6873-72del
XR_934038.1:n.6873-82_6873-72del
XM_011523918.2:c.6214-82_6214-72del XP_011522220.1:n.6214-82_6214-72del
XM_017024714.2:c.6214-82_6214-72del XP_016880203.1:n.6214-82_6214-72del
XM_017024715.2:c.6277-82_6277-72del XP_016880204.1:n.6277-82_6277-72del
XM_024450781.1:c.6213+1198_6213+1208del XP_024306549.1:n.6213+1198_6213+1208del
NM_016239.4:c.6274-82_6274-72del MANE Select NP_057323.3:n.6274-82_6274-72del