Canonical Allele Identifier: CA568152409
Gene: MYO6 HGNC NCBI

Linked Data

dbSNP Id: rs1478359448

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75913969_75913971del , CM000668.2:g.75913969_75913971del GRCh38
NC_000006.11:g.76623686_76623688del , CM000668.1:g.76623686_76623688del GRCh37
NC_000006.10:g.76680406_76680408del NCBI36
NG_009934.1:g.169778_169780del
NG_009934.2:g.169777_169779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369975.6:c.3344-94_3344-92del ENSP00000358992.1:n.3344-94_3344-92del
ENST00000369977.8:c.3440-94_3440-92del MANE Select ENSP00000358994.3:n.3440-94_3440-92del
ENST00000369985.9:c.3371-94_3371-92del ENSP00000359002.3:n.3371-94_3371-92del
ENST00000664640.1:c.3467-94_3467-92del ENSP00000499278.1:n.3467-94_3467-92del
ENST00000671923.1:c.*1451-94_*1451-92del ENSP00000500835.1:n.*1451-94_*1451-92del
ENST00000672093.1:c.3440-94_3440-92del ENSP00000500710.1:n.3440-94_3440-92del
ENST00000672162.1:n.1606-94_1606-92del
ENST00000369975.5:c.3344-94_3344-92del ENSP00000358992.1:n.3344-94_3344-92del
ENST00000369977.7:c.3440-94_3440-92del ENSP00000358994.3:n.3440-94_3440-92del
ENST00000369981.7:c.3470-94_3470-92del ENSP00000358998.4:n.3470-94_3470-92del
ENST00000369985.8:c.3371-94_3371-92del ENSP00000359002.3:n.3371-94_3371-92del
ENST00000615563.4:c.3371-94_3371-92del ENSP00000478013.1:n.3371-94_3371-92del
ENST00000627432.2:c.3467-94_3467-92del ENSP00000487348.1:n.3467-94_3467-92del
NM_001300899.1:c.3371-94_3371-92del NP_001287828.1:n.3371-94_3371-92del
NM_004999.3:c.3440-94_3440-92del NP_004990.3:n.3440-94_3440-92del
XM_005248719.2:c.3467-94_3467-92del XP_005248776.1:n.3467-94_3467-92del
XM_005248720.2:c.3440-94_3440-92del XP_005248777.1:n.3440-94_3440-92del
XM_005248721.2:c.3428-94_3428-92del XP_005248778.1:n.3428-94_3428-92del
XM_005248722.2:c.3413-94_3413-92del XP_005248779.1:n.3413-94_3413-92del
XM_005248724.2:c.3401-94_3401-92del XP_005248781.1:n.3401-94_3401-92del
XM_005248726.2:c.3344-94_3344-92del XP_005248783.1:n.3344-94_3344-92del
XM_005248719.4:c.3467-94_3467-92del XP_005248776.1:n.3467-94_3467-92del
XM_005248720.4:c.3440-94_3440-92del XP_005248777.1:n.3440-94_3440-92del
XM_005248721.4:c.3428-94_3428-92del XP_005248778.1:n.3428-94_3428-92del
XM_005248722.4:c.3413-94_3413-92del XP_005248779.1:n.3413-94_3413-92del
XM_005248724.4:c.3401-94_3401-92del XP_005248781.1:n.3401-94_3401-92del
XM_005248726.4:c.3344-94_3344-92del XP_005248783.1:n.3344-94_3344-92del
XM_017010899.2:c.3374-94_3374-92del XP_016866388.1:n.3374-94_3374-92del
XM_024446447.1:c.3467-94_3467-92del XP_024302215.1:n.3467-94_3467-92del
XM_024446448.1:c.3401-94_3401-92del XP_024302216.1:n.3401-94_3401-92del
NM_004999.4:c.3440-94_3440-92del MANE Select NP_004990.3:n.3440-94_3440-92del
NM_001300899.2:c.3371-94_3371-92del NP_001287828.1:n.3371-94_3371-92del
NM_001368136.1:c.3344-94_3344-92del NP_001355065.1:n.3344-94_3344-92del
NM_001368137.1:c.3401-94_3401-92del NP_001355066.1:n.3401-94_3401-92del
NM_001368138.1:c.3356-94_3356-92del NP_001355067.1:n.3356-94_3356-92del
NM_001368865.1:c.3467-94_3467-92del NP_001355794.1:n.3467-94_3467-92del
NM_001368866.1:c.3440-94_3440-92del NP_001355795.1:n.3440-94_3440-92del
NR_160538.1:n.3669-94_3669-92del