Canonical Allele Identifier: CA2250850211
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145722_18145724delinsCTA , CM000679.2:g.18145722_18145724delinsCTA GRCh38
NC_000017.10:g.18049036_18049038delinsCTA , CM000679.1:g.18049036_18049038delinsCTA GRCh37
NC_000017.9:g.17989761_17989763delinsCTA NCBI36
NG_011634.1:g.42017_42019delinsCTA
NG_011634.2:g.42017_42019delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-150_6274-148delinsCTA MANE Select ENSP00000495481.1:n.6274-150_6274-148delinsCTA
ENST00000205890.9:c.6274-150_6274-148delinsCTA ENSP00000205890.5:n.6274-150_6274-148delinsCTA
ENST00000615845.4:c.6274-150_6274-148delinsCTA ENSP00000481642.1:n.6274-150_6274-148delinsCTA
NM_016239.3:c.6274-150_6274-148delinsCTA NP_057323.3:n.6274-150_6274-148delinsCTA
XM_011523917.1:c.6214-150_6214-148delinsCTA XP_011522219.1:n.6214-150_6214-148delinsCTA
XM_011523918.1:c.6214-150_6214-148delinsCTA XP_011522220.1:n.6214-150_6214-148delinsCTA
XM_011523921.1:c.6268-150_6268-148delinsCTA XP_011522223.1:n.6268-150_6268-148delinsCTA
XR_934037.1:n.6873-150_6873-148delinsCTA
XR_934038.1:n.6873-150_6873-148delinsCTA
XM_011523918.2:c.6214-150_6214-148delinsCTA XP_011522220.1:n.6214-150_6214-148delinsCTA
XM_017024714.2:c.6214-150_6214-148delinsCTA XP_016880203.1:n.6214-150_6214-148delinsCTA
XM_017024715.2:c.6277-150_6277-148delinsCTA XP_016880204.1:n.6277-150_6277-148delinsCTA
XM_024450781.1:c.6213+1130_6213+1132delinsCTA XP_024306549.1:n.6213+1130_6213+1132delinsCTA
NM_016239.4:c.6274-150_6274-148delinsCTA MANE Select NP_057323.3:n.6274-150_6274-148delinsCTA
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