Canonical Allele Identifier: CA2563641964
Gene: MYO6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75859087_75859088insCTC , CM000668.2:g.75859087_75859088insCTC GRCh38
NC_000006.11:g.76568804_76568805insCTC , CM000668.1:g.76568804_76568805insCTC GRCh37
NC_000006.10:g.76625524_76625525insCTC NCBI36
NG_009934.1:g.114896_114897insCTC
NG_009934.2:g.114895_114896insCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369975.6:c.1473+94_1473+95insCTC ENSP00000358992.1:n.1473+94_1473+95insCTC
ENST00000369977.8:c.1473+94_1473+95insCTC MANE Select ENSP00000358994.3:n.1473+94_1473+95insCTC
ENST00000369985.9:c.1473+94_1473+95insCTC ENSP00000359002.3:n.1473+94_1473+95insCTC
ENST00000462633.3:c.*1029+94_*1029+95insCTC ENSP00000499616.2:n.*1029+94_*1029+95insCTC
ENST00000627432.3:c.1482+94_1482+95insCTC ENSP00000487348.2:n.1482+94_1482+95insCTC
ENST00000653423.1:c.1473+94_1473+95insCTC ENSP00000499696.1:n.1473+94_1473+95insCTC
ENST00000653917.1:c.1482+94_1482+95insCTC ENSP00000499623.1:n.1482+94_1482+95insCTC
ENST00000660420.1:c.*1429+94_*1429+95insCTC ENSP00000499263.1:n.*1429+94_*1429+95insCTC
ENST00000662184.1:c.1392+94_1392+95insCTC ENSP00000499732.1:n.1392+94_1392+95insCTC
ENST00000662603.1:c.1473+94_1473+95insCTC ENSP00000499324.1:n.1473+94_1473+95insCTC
ENST00000663400.1:c.1473+94_1473+95insCTC ENSP00000499736.1:n.1473+94_1473+95insCTC
ENST00000664209.1:c.1473+94_1473+95insCTC ENSP00000499768.1:n.1473+94_1473+95insCTC
ENST00000664640.1:c.1473+94_1473+95insCTC ENSP00000499278.1:n.1473+94_1473+95insCTC
ENST00000671923.1:c.1473+94_1473+95insCTC ENSP00000500835.1:n.1473+94_1473+95insCTC
ENST00000672093.1:c.1473+94_1473+95insCTC ENSP00000500710.1:n.1473+94_1473+95insCTC
ENST00000369975.5:c.1473+94_1473+95insCTC ENSP00000358992.1:n.1473+94_1473+95insCTC
ENST00000369977.7:c.1473+94_1473+95insCTC ENSP00000358994.3:n.1473+94_1473+95insCTC
ENST00000369981.7:c.1473+94_1473+95insCTC ENSP00000358998.4:n.1473+94_1473+95insCTC
ENST00000369985.8:c.1473+94_1473+95insCTC ENSP00000359002.3:n.1473+94_1473+95insCTC
ENST00000615563.4:c.1473+94_1473+95insCTC ENSP00000478013.1:n.1473+94_1473+95insCTC
ENST00000627432.2:c.1473+94_1473+95insCTC ENSP00000487348.1:n.1473+94_1473+95insCTC
NM_001300899.1:c.1473+94_1473+95insCTC NP_001287828.1:n.1473+94_1473+95insCTC
NM_004999.3:c.1473+94_1473+95insCTC NP_004990.3:n.1473+94_1473+95insCTC
XM_005248719.2:c.1473+94_1473+95insCTC XP_005248776.1:n.1473+94_1473+95insCTC
XM_005248720.2:c.1473+94_1473+95insCTC XP_005248777.1:n.1473+94_1473+95insCTC
XM_005248721.2:c.1473+94_1473+95insCTC XP_005248778.1:n.1473+94_1473+95insCTC
XM_005248722.2:c.1473+94_1473+95insCTC XP_005248779.1:n.1473+94_1473+95insCTC
XM_005248724.2:c.1473+94_1473+95insCTC XP_005248781.1:n.1473+94_1473+95insCTC
XM_005248726.2:c.1473+94_1473+95insCTC XP_005248783.1:n.1473+94_1473+95insCTC
XM_005248719.4:c.1473+94_1473+95insCTC XP_005248776.1:n.1473+94_1473+95insCTC
XM_005248720.4:c.1473+94_1473+95insCTC XP_005248777.1:n.1473+94_1473+95insCTC
XM_005248721.4:c.1473+94_1473+95insCTC XP_005248778.1:n.1473+94_1473+95insCTC
XM_005248722.4:c.1473+94_1473+95insCTC XP_005248779.1:n.1473+94_1473+95insCTC
XM_005248724.4:c.1473+94_1473+95insCTC XP_005248781.1:n.1473+94_1473+95insCTC
XM_005248726.4:c.1473+94_1473+95insCTC XP_005248783.1:n.1473+94_1473+95insCTC
XM_017010899.2:c.1473+94_1473+95insCTC XP_016866388.1:n.1473+94_1473+95insCTC
XM_024446447.1:c.1473+94_1473+95insCTC XP_024302215.1:n.1473+94_1473+95insCTC
XM_024446448.1:c.1473+94_1473+95insCTC XP_024302216.1:n.1473+94_1473+95insCTC
NM_004999.4:c.1473+94_1473+95insCTC MANE Select NP_004990.3:n.1473+94_1473+95insCTC
NM_001300899.2:c.1473+94_1473+95insCTC NP_001287828.1:n.1473+94_1473+95insCTC
NM_001368136.1:c.1473+94_1473+95insCTC NP_001355065.1:n.1473+94_1473+95insCTC
NM_001368137.1:c.1473+94_1473+95insCTC NP_001355066.1:n.1473+94_1473+95insCTC
NM_001368138.1:c.1458+94_1458+95insCTC NP_001355067.1:n.1458+94_1458+95insCTC
NM_001368865.1:c.1473+94_1473+95insCTC NP_001355794.1:n.1473+94_1473+95insCTC
NM_001368866.1:c.1473+94_1473+95insCTC NP_001355795.1:n.1473+94_1473+95insCTC
NR_160538.1:n.1705+94_1705+95insCTC