Canonical Allele Identifier: CA2250868982
Community Standard Title: NM_016239.4(MYO15A):c.8714-1G=
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18157155G= , CM000679.2:g.18157155G= GRCh38
NC_000017.10:g.18060469G= , CM000679.1:g.18060469G= GRCh37
NC_000017.9:g.18001194G= NCBI36
NG_011634.1:g.53450G=
NG_011634.2:g.53450G=

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.8714-1G= MANE Select NP_057323.3:n.8714-1G=
ENST00000647165.2:c.8714-1G= MANE Select ENSP00000495481.1:n.8714-1G=
NM_016239.3:c.8714-1G= NP_057323.3:n.8714-1G=
ENST00000205890.9:c.8714-1G= ENSP00000205890.5:n.8714-1G=
ENST00000418233.7:c.506-1G= ENSP00000408800.3:n.506-1G=
ENST00000445289.6:n.138-567G=
ENST00000536811.5:n.627-1G=
ENST00000615845.4:c.8714-1G= ENSP00000481642.1:n.8714-1G=
ENST00000642418.1:n.561-1G=
ENST00000643693.1:n.534-1G=
ENST00000644795.1:c.506-1G= ENSP00000495720.1:n.506-1G=
ENST00000646782.1:n.957-1G=
ENST00000651214.1:n.860-1G=
XM_011523921.1:c.8708-1G= XP_011522223.1:n.8708-1G=
XM_017024714.2:c.8654-1G= XP_016880203.1:n.8654-1G=
XM_017024715.2:c.8717-1G= XP_016880204.1:n.8717-1G=