Canonical Allele Identifier: CA2250850384
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146110G= , CM000679.2:g.18146110G= GRCh38
NC_000017.10:g.18049424G= , CM000679.1:g.18049424G= GRCh37
NC_000017.9:g.17990149G= NCBI36
NG_011634.1:g.42405G=
NG_011634.2:g.42405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6509+3G= MANE Select ENSP00000495481.1:n.6509+3G=
ENST00000205890.9:c.6509+3G= ENSP00000205890.5:n.6509+3G=
ENST00000578999.1:n.94+3G=
ENST00000615845.4:c.6509+3G= ENSP00000481642.1:n.6509+3G=
NM_016239.3:c.6509+3G= NP_057323.3:n.6509+3G=
XM_011523917.1:c.6449+3G= XP_011522219.1:n.6449+3G=
XM_011523918.1:c.6342+110G= XP_011522220.1:n.6342+110G=
XM_011523921.1:c.6503+3G= XP_011522223.1:n.6503+3G=
XR_934037.1:n.7108+3G=
XR_934038.1:n.7108+3G=
XM_011523918.2:c.6342+110G= XP_011522220.1:n.6342+110G=
XM_017024714.2:c.6449+3G= XP_016880203.1:n.6449+3G=
XM_017024715.2:c.6512+3G= XP_016880204.1:n.6512+3G=
XM_024450781.1:c.6213+1518G= XP_024306549.1:n.6213+1518G=
NM_016239.4:c.6509+3G= MANE Select NP_057323.3:n.6509+3G=
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