Canonical Allele Identifier: CA2250850408
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146153C= , CM000679.2:g.18146153C= GRCh38
NC_000017.10:g.18049467C= , CM000679.1:g.18049467C= GRCh37
NC_000017.9:g.17990192C= NCBI36
NG_011634.1:g.42448C=
NG_011634.2:g.42448C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6509+46C= MANE Select ENSP00000495481.1:n.6509+46C=
ENST00000205890.9:c.6509+46C= ENSP00000205890.5:n.6509+46C=
ENST00000578999.1:n.94+46C=
ENST00000615845.4:c.6509+46C= ENSP00000481642.1:n.6509+46C=
NM_016239.3:c.6509+46C= NP_057323.3:n.6509+46C=
XM_011523917.1:c.6449+46C= XP_011522219.1:n.6449+46C=
XM_011523918.1:c.6342+153C= XP_011522220.1:n.6342+153C=
XM_011523921.1:c.6503+46C= XP_011522223.1:n.6503+46C=
XR_934037.1:n.7108+46C=
XR_934038.1:n.7108+46C=
XM_011523918.2:c.6342+153C= XP_011522220.1:n.6342+153C=
XM_017024714.2:c.6449+46C= XP_016880203.1:n.6449+46C=
XM_017024715.2:c.6512+46C= XP_016880204.1:n.6512+46C=
XM_024450781.1:c.6213+1561C= XP_024306549.1:n.6213+1561C=
NM_016239.4:c.6509+46C= MANE Select NP_057323.3:n.6509+46C=