Canonical Allele Identifier: CA2250850297
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145891A= , CM000679.2:g.18145891A= GRCh38
NC_000017.10:g.18049205A= , CM000679.1:g.18049205A= GRCh37
NC_000017.9:g.17989930A= NCBI36
NG_011634.1:g.42186A=
NG_011634.2:g.42186A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6293A= MANE Select ENSP00000495481.1:p.Asp2098=
ENST00000205890.9:c.6293A= ENSP00000205890.5:p.Asp2098=
ENST00000615845.4:c.6293A= ENSP00000481642.1:p.Asp2098=
NM_016239.3:c.6293A= NP_057323.3:p.Asp2098=
XM_011523917.1:c.6233A= XP_011522219.1:p.Asp2078=
XM_011523918.1:c.6233A= XP_011522220.1:p.Asp2078=
XM_011523921.1:c.6287A= XP_011522223.1:p.Asp2096=
XR_934037.1:n.6892A=
XR_934038.1:n.6892A=
XM_011523918.2:c.6233A= XP_011522220.1:p.Asp2078=
XM_017024714.2:c.6233A= XP_016880203.1:p.Asp2078=
XM_017024715.2:c.6296A= XP_016880204.1:p.Asp2099=
XM_024450781.1:c.6213+1299A= XP_024306549.1:n.6213+1299A=
NM_016239.4:c.6293A= MANE Select NP_057323.3:p.Asp2098=