Canonical Allele Identifier: CA2840524796
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145888dup , CM000679.2:g.18145888dup GRCh38
NC_000017.10:g.18049202dup , CM000679.1:g.18049202dup GRCh37
NC_000017.9:g.17989927dup NCBI36
NG_011634.1:g.42183dup
NG_011634.2:g.42183dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6290dup MANE Select ENSP00000495481.1:p.Asp2098ArgfsTer25
ENST00000205890.9:c.6290dup ENSP00000205890.5:p.Asp2098ArgfsTer25
ENST00000615845.4:c.6290dup ENSP00000481642.1:p.Asp2098ArgfsTer25
NM_016239.3:c.6290dup NP_057323.3:p.Asp2098ArgfsTer25
XM_011523917.1:c.6230dup XP_011522219.1:p.Asp2078ArgfsTer25
XM_011523918.1:c.6230dup XP_011522220.1:p.Asp2078ArgfsTer25
XM_011523921.1:c.6284dup XP_011522223.1:p.Asp2096ArgfsTer25
XR_934037.1:n.6889dup
XR_934038.1:n.6889dup
XM_011523918.2:c.6230dup XP_011522220.1:p.Asp2078ArgfsTer25
XM_017024714.2:c.6230dup XP_016880203.1:p.Asp2078ArgfsTer25
XM_017024715.2:c.6293dup XP_016880204.1:p.Asp2099ArgfsTer25
XM_024450781.1:c.6213+1296dup XP_024306549.1:n.6213+1296dup
NM_016239.4:c.6290dup MANE Select NP_057323.3:p.Asp2098ArgfsTer25
Search 100 bp 5'
Search 100 bp 3'