Canonical Allele Identifier: CA2695224488
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145906dup , CM000679.2:g.18145906dup GRCh38
NC_000017.10:g.18049220dup , CM000679.1:g.18049220dup GRCh37
NC_000017.9:g.17989945dup NCBI36
NG_011634.1:g.42201dup
NG_011634.2:g.42201dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6308dup MANE Select ENSP00000495481.1:p.Ala2104CysfsTer19
ENST00000205890.9:c.6308dup ENSP00000205890.5:p.Ala2104CysfsTer19
ENST00000615845.4:c.6308dup ENSP00000481642.1:p.Ala2104CysfsTer19
NM_016239.3:c.6308dup NP_057323.3:p.Ala2104CysfsTer19
XM_011523917.1:c.6248dup XP_011522219.1:p.Ala2084CysfsTer19
XM_011523918.1:c.6248dup XP_011522220.1:p.Ala2084CysfsTer19
XM_011523921.1:c.6302dup XP_011522223.1:p.Ala2102CysfsTer19
XR_934037.1:n.6907dup
XR_934038.1:n.6907dup
XM_011523918.2:c.6248dup XP_011522220.1:p.Ala2084CysfsTer19
XM_017024714.2:c.6248dup XP_016880203.1:p.Ala2084CysfsTer19
XM_017024715.2:c.6311dup XP_016880204.1:p.Ala2105CysfsTer19
XM_024450781.1:c.6213+1314dup XP_024306549.1:n.6213+1314dup
NM_016239.4:c.6308dup MANE Select NP_057323.3:p.Ala2104CysfsTer19
Search 100 bp 5'
Search 100 bp 3'