Canonical Allele Identifier: CA2250850175
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs2046462625
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145658_18145659del , CM000679.2:g.18145658_18145659del GRCh38
NC_000017.10:g.18048972_18048973del , CM000679.1:g.18048972_18048973del GRCh37
NC_000017.9:g.17989697_17989698del NCBI36
NG_011634.1:g.41953_41954del
NG_011634.2:g.41953_41954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-214_6274-213del MANE Select ENSP00000495481.1:n.6274-214_6274-213del
ENST00000205890.9:c.6274-214_6274-213del ENSP00000205890.5:n.6274-214_6274-213del
ENST00000615845.4:c.6274-214_6274-213del ENSP00000481642.1:n.6274-214_6274-213del
NM_016239.3:c.6274-214_6274-213del NP_057323.3:n.6274-214_6274-213del
XM_011523917.1:c.6214-214_6214-213del XP_011522219.1:n.6214-214_6214-213del
XM_011523918.1:c.6214-214_6214-213del XP_011522220.1:n.6214-214_6214-213del
XM_011523921.1:c.6268-214_6268-213del XP_011522223.1:n.6268-214_6268-213del
XR_934037.1:n.6873-214_6873-213del
XR_934038.1:n.6873-214_6873-213del
XM_011523918.2:c.6214-214_6214-213del XP_011522220.1:n.6214-214_6214-213del
XM_017024714.2:c.6214-214_6214-213del XP_016880203.1:n.6214-214_6214-213del
XM_017024715.2:c.6277-214_6277-213del XP_016880204.1:n.6277-214_6277-213del
XM_024450781.1:c.6213+1066_6213+1067del XP_024306549.1:n.6213+1066_6213+1067del
NM_016239.4:c.6274-214_6274-213del MANE Select NP_057323.3:n.6274-214_6274-213del
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