Canonical Allele Identifier: CA2497157165
Gene: MYO6 HGNC NCBI

Linked Data

dbSNP Id: rs1304981195

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75918915_75918916insCC , CM000668.2:g.75918915_75918916insCC GRCh38
NC_000006.11:g.76628632_76628633insCC , CM000668.1:g.76628632_76628633insCC GRCh37
NC_000006.10:g.76685352_76685353insCC NCBI36
NG_009934.1:g.174724_174725insCC
NG_009934.2:g.174723_174724insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369977.8:c.*3903_*3904insCC MANE Select ENSP00000358994.3:n.*3903_*3904insCC
ENST00000369985.9:c.*3903_*3904insCC ENSP00000359002.3:n.*3903_*3904insCC
ENST00000664640.1:c.*3903_*3904insCC ENSP00000499278.1:n.*3903_*3904insCC
ENST00000369981.7:c.*3903_*3904insCC ENSP00000358998.4:n.*3903_*3904insCC
ENST00000369985.8:c.*3903_*3904insCC ENSP00000359002.3:n.*3903_*3904insCC
NM_001300899.1:c.*3903_*3904insCC NP_001287828.1:n.*3903_*3904insCC
NM_004999.3:c.*3903_*3904insCC NP_004990.3:n.*3903_*3904insCC
XM_005248719.4:c.*3903_*3904insCC XP_005248776.1:n.*3903_*3904insCC
XM_005248720.4:c.*3903_*3904insCC XP_005248777.1:n.*3903_*3904insCC
XM_005248721.4:c.*3903_*3904insCC XP_005248778.1:n.*3903_*3904insCC
XM_005248722.4:c.*3903_*3904insCC XP_005248779.1:n.*3903_*3904insCC
XM_005248724.4:c.*3903_*3904insCC XP_005248781.1:n.*3903_*3904insCC
XM_005248726.4:c.*3903_*3904insCC XP_005248783.1:n.*3903_*3904insCC
XM_017010899.2:c.*3903_*3904insCC XP_016866388.1:n.*3903_*3904insCC
XM_024446447.1:c.*3903_*3904insCC XP_024302215.1:n.*3903_*3904insCC
XM_024446448.1:c.*3903_*3904insCC XP_024302216.1:n.*3903_*3904insCC
NM_004999.4:c.*3903_*3904insCC MANE Select NP_004990.3:n.*3903_*3904insCC
NM_001300899.2:c.*3903_*3904insCC NP_001287828.1:n.*3903_*3904insCC
NM_001368136.1:c.*3903_*3904insCC NP_001355065.1:n.*3903_*3904insCC
NM_001368137.1:c.*3903_*3904insCC NP_001355066.1:n.*3903_*3904insCC
NM_001368138.1:c.*3903_*3904insCC NP_001355067.1:n.*3903_*3904insCC
NM_001368865.1:c.*3903_*3904insCC NP_001355794.1:n.*3903_*3904insCC
NM_001368866.1:c.*3903_*3904insCC NP_001355795.1:n.*3903_*3904insCC
NR_160538.1:n.7990_7991insCC