Canonical Allele Identifier: CA2250850372
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146079_18146080delinsTC , CM000679.2:g.18146079_18146080delinsTC GRCh38
NC_000017.10:g.18049393_18049394delinsTC , CM000679.1:g.18049393_18049394delinsTC GRCh37
NC_000017.9:g.17990118_17990119delinsTC NCBI36
NG_011634.1:g.42374_42375delinsTC
NG_011634.2:g.42374_42375delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6481_6482delinsTC MANE Select ENSP00000495481.1:p.Ser2161=
ENST00000205890.9:c.6481_6482delinsTC ENSP00000205890.5:p.Ser2161=
ENST00000578999.1:n.66_67delinsTC
ENST00000615845.4:c.6481_6482delinsTC ENSP00000481642.1:p.Ser2161=
NM_016239.3:c.6481_6482delinsTC NP_057323.3:p.Ser2161=
XM_011523917.1:c.6421_6422delinsTC XP_011522219.1:p.Ser2141=
XM_011523918.1:c.6342+79_6342+80delinsTC XP_011522220.1:n.6342+79_6342+80delinsTC
XM_011523921.1:c.6475_6476delinsTC XP_011522223.1:p.Ser2159=
XR_934037.1:n.7080_7081delinsTC
XR_934038.1:n.7080_7081delinsTC
XM_011523918.2:c.6342+79_6342+80delinsTC XP_011522220.1:n.6342+79_6342+80delinsTC
XM_017024714.2:c.6421_6422delinsTC XP_016880203.1:p.Ser2141=
XM_017024715.2:c.6484_6485delinsTC XP_016880204.1:p.Ser2162=
XM_024450781.1:c.6213+1487_6213+1488delinsTC XP_024306549.1:n.6213+1487_6213+1488delinsTC
NM_016239.4:c.6481_6482delinsTC MANE Select NP_057323.3:p.Ser2161=
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