Canonical Allele Identifier: CA2963287819
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145914dup , CM000679.2:g.18145914dup GRCh38
NC_000017.10:g.18049228dup , CM000679.1:g.18049228dup GRCh37
NC_000017.9:g.17989953dup NCBI36
NG_011634.1:g.42209dup
NG_011634.2:g.42209dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6316dup MANE Select ENSP00000495481.1:p.Glu2106GlyfsTer17
ENST00000205890.9:c.6316dup ENSP00000205890.5:p.Glu2106GlyfsTer17
ENST00000615845.4:c.6316dup ENSP00000481642.1:p.Glu2106GlyfsTer17
NM_016239.3:c.6316dup NP_057323.3:p.Glu2106GlyfsTer17
XM_011523917.1:c.6256dup XP_011522219.1:p.Glu2086GlyfsTer17
XM_011523918.1:c.6256dup XP_011522220.1:p.Glu2086GlyfsTer17
XM_011523921.1:c.6310dup XP_011522223.1:p.Glu2104GlyfsTer17
XR_934037.1:n.6915dup
XR_934038.1:n.6915dup
XM_011523918.2:c.6256dup XP_011522220.1:p.Glu2086GlyfsTer17
XM_017024714.2:c.6256dup XP_016880203.1:p.Glu2086GlyfsTer17
XM_017024715.2:c.6319dup XP_016880204.1:p.Glu2107GlyfsTer17
XM_024450781.1:c.6213+1322dup XP_024306549.1:n.6213+1322dup
NM_016239.4:c.6316dup MANE Select NP_057323.3:p.Glu2106GlyfsTer17
Search 100 bp 5'
Search 100 bp 3'