Canonical Allele Identifier: CA2250850368
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146065G= , CM000679.2:g.18146065G= GRCh38
NC_000017.10:g.18049379G= , CM000679.1:g.18049379G= GRCh37
NC_000017.9:g.17990104G= NCBI36
NG_011634.1:g.42360G=
NG_011634.2:g.42360G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6467G= MANE Select ENSP00000495481.1:p.Ser2156=
ENST00000205890.9:c.6467G= ENSP00000205890.5:p.Ser2156=
ENST00000578999.1:n.52G=
ENST00000615845.4:c.6467G= ENSP00000481642.1:p.Ser2156=
NM_016239.3:c.6467G= NP_057323.3:p.Ser2156=
XM_011523917.1:c.6407G= XP_011522219.1:p.Ser2136=
XM_011523918.1:c.6342+65G= XP_011522220.1:n.6342+65G=
XM_011523921.1:c.6461G= XP_011522223.1:p.Ser2154=
XR_934037.1:n.7066G=
XR_934038.1:n.7066G=
XM_011523918.2:c.6342+65G= XP_011522220.1:n.6342+65G=
XM_017024714.2:c.6407G= XP_016880203.1:p.Ser2136=
XM_017024715.2:c.6470G= XP_016880204.1:p.Ser2157=
XM_024450781.1:c.6213+1473G= XP_024306549.1:n.6213+1473G=
NM_016239.4:c.6467G= MANE Select NP_057323.3:p.Ser2156=