Canonical Allele Identifier: CA2250850339
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145969G= , CM000679.2:g.18145969G= GRCh38
NC_000017.10:g.18049283G= , CM000679.1:g.18049283G= GRCh37
NC_000017.9:g.17990008G= NCBI36
NG_011634.1:g.42264G=
NG_011634.2:g.42264G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6371G= MANE Select ENSP00000495481.1:p.Arg2124=
ENST00000205890.9:c.6371G= ENSP00000205890.5:p.Arg2124=
ENST00000615845.4:c.6371G= ENSP00000481642.1:p.Arg2124=
NM_016239.3:c.6371G= NP_057323.3:p.Arg2124=
XM_011523917.1:c.6311G= XP_011522219.1:p.Arg2104=
XM_011523918.1:c.6311G= XP_011522220.1:p.Arg2104=
XM_011523921.1:c.6365G= XP_011522223.1:p.Arg2122=
XR_934037.1:n.6970G=
XR_934038.1:n.6970G=
XM_011523918.2:c.6311G= XP_011522220.1:p.Arg2104=
XM_017024714.2:c.6311G= XP_016880203.1:p.Arg2104=
XM_017024715.2:c.6374G= XP_016880204.1:p.Arg2125=
XM_024450781.1:c.6213+1377G= XP_024306549.1:n.6213+1377G=
NM_016239.4:c.6371G= MANE Select NP_057323.3:p.Arg2124=