Canonical Allele Identifier: CA2250850350
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146010A= , CM000679.2:g.18146010A= GRCh38
NC_000017.10:g.18049324A= , CM000679.1:g.18049324A= GRCh37
NC_000017.9:g.17990049A= NCBI36
NG_011634.1:g.42305A=
NG_011634.2:g.42305A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6412A= MANE Select ENSP00000495481.1:p.Asn2138=
ENST00000205890.9:c.6412A= ENSP00000205890.5:p.Asn2138=
ENST00000615845.4:c.6412A= ENSP00000481642.1:p.Asn2138=
NM_016239.3:c.6412A= NP_057323.3:p.Asn2138=
XM_011523917.1:c.6352A= XP_011522219.1:p.Asn2118=
XM_011523918.1:c.6342+10A= XP_011522220.1:n.6342+10A=
XM_011523921.1:c.6406A= XP_011522223.1:p.Asn2136=
XR_934037.1:n.7011A=
XR_934038.1:n.7011A=
XM_011523918.2:c.6342+10A= XP_011522220.1:n.6342+10A=
XM_017024714.2:c.6352A= XP_016880203.1:p.Asn2118=
XM_017024715.2:c.6415A= XP_016880204.1:p.Asn2139=
XM_024450781.1:c.6213+1418A= XP_024306549.1:n.6213+1418A=
NM_016239.4:c.6412A= MANE Select NP_057323.3:p.Asn2138=