Canonical Allele Identifier: CA2576190379
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145799_18145803dup , CM000679.2:g.18145799_18145803dup GRCh38
NC_000017.10:g.18049113_18049117dup , CM000679.1:g.18049113_18049117dup GRCh37
NC_000017.9:g.17989838_17989842dup NCBI36
NG_011634.1:g.42094_42098dup
NG_011634.2:g.42094_42098dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-73_6274-69dup MANE Select ENSP00000495481.1:n.6274-73_6274-69dup
ENST00000205890.9:c.6274-73_6274-69dup ENSP00000205890.5:n.6274-73_6274-69dup
ENST00000615845.4:c.6274-73_6274-69dup ENSP00000481642.1:n.6274-73_6274-69dup
NM_016239.3:c.6274-73_6274-69dup NP_057323.3:n.6274-73_6274-69dup
XM_011523917.1:c.6214-73_6214-69dup XP_011522219.1:n.6214-73_6214-69dup
XM_011523918.1:c.6214-73_6214-69dup XP_011522220.1:n.6214-73_6214-69dup
XM_011523921.1:c.6268-73_6268-69dup XP_011522223.1:n.6268-73_6268-69dup
XR_934037.1:n.6873-73_6873-69dup
XR_934038.1:n.6873-73_6873-69dup
XM_011523918.2:c.6214-73_6214-69dup XP_011522220.1:n.6214-73_6214-69dup
XM_017024714.2:c.6214-73_6214-69dup XP_016880203.1:n.6214-73_6214-69dup
XM_017024715.2:c.6277-73_6277-69dup XP_016880204.1:n.6277-73_6277-69dup
XM_024450781.1:c.6213+1207_6213+1211dup XP_024306549.1:n.6213+1207_6213+1211dup
NM_016239.4:c.6274-73_6274-69dup MANE Select NP_057323.3:n.6274-73_6274-69dup
Search 100 bp 5'
Search 100 bp 3'