Canonical Allele Identifier: CA2250850360
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146047T= , CM000679.2:g.18146047T= GRCh38
NC_000017.10:g.18049361T= , CM000679.1:g.18049361T= GRCh37
NC_000017.9:g.17990086T= NCBI36
NG_011634.1:g.42342T=
NG_011634.2:g.42342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6449T= MANE Select ENSP00000495481.1:p.Leu2150=
ENST00000205890.9:c.6449T= ENSP00000205890.5:p.Leu2150=
ENST00000578999.1:n.34T=
ENST00000615845.4:c.6449T= ENSP00000481642.1:p.Leu2150=
NM_016239.3:c.6449T= NP_057323.3:p.Leu2150=
XM_011523917.1:c.6389T= XP_011522219.1:p.Leu2130=
XM_011523918.1:c.6342+47T= XP_011522220.1:n.6342+47T=
XM_011523921.1:c.6443T= XP_011522223.1:p.Leu2148=
XR_934037.1:n.7048T=
XR_934038.1:n.7048T=
XM_011523918.2:c.6342+47T= XP_011522220.1:n.6342+47T=
XM_017024714.2:c.6389T= XP_016880203.1:p.Leu2130=
XM_017024715.2:c.6452T= XP_016880204.1:p.Leu2151=
XM_024450781.1:c.6213+1455T= XP_024306549.1:n.6213+1455T=
NM_016239.4:c.6449T= MANE Select NP_057323.3:p.Leu2150=