Canonical Allele Identifier: CA2636447559
Gene: MYO15A HGNC NCBI

Linked Data

gnomAD v4: 17-18145822-TGGAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145827_18145830del , CM000679.2:g.18145827_18145830del GRCh38
NC_000017.10:g.18049141_18049144del , CM000679.1:g.18049141_18049144del GRCh37
NC_000017.9:g.17989866_17989869del NCBI36
NG_011634.1:g.42122_42125del
NG_011634.2:g.42122_42125del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-45_6274-42del MANE Select ENSP00000495481.1:n.6274-45_6274-42del
ENST00000205890.9:c.6274-45_6274-42del ENSP00000205890.5:n.6274-45_6274-42del
ENST00000615845.4:c.6274-45_6274-42del ENSP00000481642.1:n.6274-45_6274-42del
NM_016239.3:c.6274-45_6274-42del NP_057323.3:n.6274-45_6274-42del
XM_011523917.1:c.6214-45_6214-42del XP_011522219.1:n.6214-45_6214-42del
XM_011523918.1:c.6214-45_6214-42del XP_011522220.1:n.6214-45_6214-42del
XM_011523921.1:c.6268-45_6268-42del XP_011522223.1:n.6268-45_6268-42del
XR_934037.1:n.6873-45_6873-42del
XR_934038.1:n.6873-45_6873-42del
XM_011523918.2:c.6214-45_6214-42del XP_011522220.1:n.6214-45_6214-42del
XM_017024714.2:c.6214-45_6214-42del XP_016880203.1:n.6214-45_6214-42del
XM_017024715.2:c.6277-45_6277-42del XP_016880204.1:n.6277-45_6277-42del
XM_024450781.1:c.6213+1235_6213+1238del XP_024306549.1:n.6213+1235_6213+1238del
NM_016239.4:c.6274-45_6274-42del MANE Select NP_057323.3:n.6274-45_6274-42del
Search 100 bp 5'
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