Canonical Allele Identifier: CA2250850177
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145663T= , CM000679.2:g.18145663T= GRCh38
NC_000017.10:g.18048977T= , CM000679.1:g.18048977T= GRCh37
NC_000017.9:g.17989702T= NCBI36
NG_011634.1:g.41958T=
NG_011634.2:g.41958T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-209T= MANE Select ENSP00000495481.1:n.6274-209T=
ENST00000205890.9:c.6274-209T= ENSP00000205890.5:n.6274-209T=
ENST00000615845.4:c.6274-209T= ENSP00000481642.1:n.6274-209T=
NM_016239.3:c.6274-209T= NP_057323.3:n.6274-209T=
XM_011523917.1:c.6214-209T= XP_011522219.1:n.6214-209T=
XM_011523918.1:c.6214-209T= XP_011522220.1:n.6214-209T=
XM_011523921.1:c.6268-209T= XP_011522223.1:n.6268-209T=
XR_934037.1:n.6873-209T=
XR_934038.1:n.6873-209T=
XM_011523918.2:c.6214-209T= XP_011522220.1:n.6214-209T=
XM_017024714.2:c.6214-209T= XP_016880203.1:n.6214-209T=
XM_017024715.2:c.6277-209T= XP_016880204.1:n.6277-209T=
XM_024450781.1:c.6213+1071T= XP_024306549.1:n.6213+1071T=
NM_016239.4:c.6274-209T= MANE Select NP_057323.3:n.6274-209T=