Canonical Allele Identifier: CA2576190377
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145796_18145797del , CM000679.2:g.18145796_18145797del GRCh38
NC_000017.10:g.18049110_18049111del , CM000679.1:g.18049110_18049111del GRCh37
NC_000017.9:g.17989835_17989836del NCBI36
NG_011634.1:g.42091_42092del
NG_011634.2:g.42091_42092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-76_6274-75del MANE Select ENSP00000495481.1:n.6274-76_6274-75del
ENST00000205890.9:c.6274-76_6274-75del ENSP00000205890.5:n.6274-76_6274-75del
ENST00000615845.4:c.6274-76_6274-75del ENSP00000481642.1:n.6274-76_6274-75del
NM_016239.3:c.6274-76_6274-75del NP_057323.3:n.6274-76_6274-75del
XM_011523917.1:c.6214-76_6214-75del XP_011522219.1:n.6214-76_6214-75del
XM_011523918.1:c.6214-76_6214-75del XP_011522220.1:n.6214-76_6214-75del
XM_011523921.1:c.6268-76_6268-75del XP_011522223.1:n.6268-76_6268-75del
XR_934037.1:n.6873-76_6873-75del
XR_934038.1:n.6873-76_6873-75del
XM_011523918.2:c.6214-76_6214-75del XP_011522220.1:n.6214-76_6214-75del
XM_017024714.2:c.6214-76_6214-75del XP_016880203.1:n.6214-76_6214-75del
XM_017024715.2:c.6277-76_6277-75del XP_016880204.1:n.6277-76_6277-75del
XM_024450781.1:c.6213+1204_6213+1205del XP_024306549.1:n.6213+1204_6213+1205del
NM_016239.4:c.6274-76_6274-75del MANE Select NP_057323.3:n.6274-76_6274-75del