Canonical Allele Identifier: CA2695224489

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145945del , CM000679.2:g.18145945del	GRCh38
NC_000017.10:g.18049259del , CM000679.1:g.18049259del	GRCh37
NC_000017.9:g.17989984del	NCBI36
NG_011634.1:g.42240del
NG_011634.2:g.42240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6347del MANE Select	ENSP00000495481.1:p.Lys2116ArgfsTer?
ENST00000205890.9:c.6347del	ENSP00000205890.5:p.Lys2116ArgfsTer?
ENST00000615845.4:c.6347del	ENSP00000481642.1:p.Lys2116ArgfsTer?
NM_016239.3:c.6347del	NP_057323.3:p.Lys2116ArgfsTer?
XM_011523917.1:c.6287del	XP_011522219.1:p.Lys2096ArgfsTer?
XM_011523918.1:c.6287del	XP_011522220.1:p.Lys2096ArgfsTer?
XM_011523921.1:c.6341del	XP_011522223.1:p.Lys2114ArgfsTer?
XR_934037.1:n.6946del
XR_934038.1:n.6946del
XM_011523918.2:c.6287del	XP_011522220.1:p.Lys2096ArgfsTer?
XM_017024714.2:c.6287del	XP_016880203.1:p.Lys2096ArgfsTer?
XM_017024715.2:c.6350del	XP_016880204.1:p.Lys2117ArgfsTer?
XM_024450781.1:c.6213+1353del	XP_024306549.1:n.6213+1353del
NM_016239.4:c.6347del MANE Select	NP_057323.3:p.Lys2116ArgfsTer?