Canonical Allele Identifier: CA2250850367
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146064A= , CM000679.2:g.18146064A= GRCh38
NC_000017.10:g.18049378A= , CM000679.1:g.18049378A= GRCh37
NC_000017.9:g.17990103A= NCBI36
NG_011634.1:g.42359A=
NG_011634.2:g.42359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6466A= MANE Select ENSP00000495481.1:p.Ser2156=
ENST00000205890.9:c.6466A= ENSP00000205890.5:p.Ser2156=
ENST00000578999.1:n.51A=
ENST00000615845.4:c.6466A= ENSP00000481642.1:p.Ser2156=
NM_016239.3:c.6466A= NP_057323.3:p.Ser2156=
XM_011523917.1:c.6406A= XP_011522219.1:p.Ser2136=
XM_011523918.1:c.6342+64A= XP_011522220.1:n.6342+64A=
XM_011523921.1:c.6460A= XP_011522223.1:p.Ser2154=
XR_934037.1:n.7065A=
XR_934038.1:n.7065A=
XM_011523918.2:c.6342+64A= XP_011522220.1:n.6342+64A=
XM_017024714.2:c.6406A= XP_016880203.1:p.Ser2136=
XM_017024715.2:c.6469A= XP_016880204.1:p.Ser2157=
XM_024450781.1:c.6213+1472A= XP_024306549.1:n.6213+1472A=
NM_016239.4:c.6466A= MANE Select NP_057323.3:p.Ser2156=