Canonical Allele Identifier: CA3897741

Gene: MYO6

Linked Data

• dbSNP Id: rs775976856
• ExAC: 6:76623818 C / T
• gnomAD v2: 6-76623818-C-T
• gnomAD v3: 6-75914101-C-T
• gnomAD v4: 6-75914101-C-T
• MyVariant Identifiers: chr6:g.76623818C>T (hg19) ; chr6:g.75914101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914101C>T , CM000668.2:g.75914101C>T	GRCh38
NC_000006.11:g.76623818C>T , CM000668.1:g.76623818C>T	GRCh37
NC_000006.10:g.76680538C>T	NCBI36
NG_009934.1:g.169910C>T
NG_009934.2:g.169909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3382C>T	ENSP00000358992.1:p.Arg1128Trp
ENST00000369977.8:c.3478C>T MANE Select	ENSP00000358994.3:p.Arg1160Trp
ENST00000369985.9:c.3409C>T	ENSP00000359002.3:p.Arg1137Trp
ENST00000664640.1:c.3505C>T	ENSP00000499278.1:p.Arg1169Trp
ENST00000671923.1:c.*1489C>T	ENSP00000500835.1:n.*1489C>T
ENST00000672093.1:c.3478C>T	ENSP00000500710.1:p.Arg1160Trp
ENST00000672162.1:n.1644C>T
ENST00000369975.5:c.3382C>T	ENSP00000358992.1:p.Arg1128Trp
ENST00000369977.7:c.3478C>T	ENSP00000358994.3:p.Arg1160Trp
ENST00000369981.7:c.3508C>T	ENSP00000358998.4:p.Arg1170Trp
ENST00000369985.8:c.3409C>T	ENSP00000359002.3:p.Arg1137Trp
ENST00000615563.4:c.3409C>T	ENSP00000478013.1:p.Arg1137Trp
ENST00000627432.2:c.3505C>T	ENSP00000487348.1:p.Arg1169Trp
NM_001300899.1:c.3409C>T	NP_001287828.1:p.Arg1137Trp
NM_004999.3:c.3478C>T	NP_004990.3:p.Arg1160Trp
XM_005248719.2:c.3505C>T	XP_005248776.1:p.Arg1169Trp
XM_005248720.2:c.3478C>T	XP_005248777.1:p.Arg1160Trp
XM_005248721.2:c.3466C>T	XP_005248778.1:p.Arg1156Trp
XM_005248722.2:c.3451C>T	XP_005248779.1:p.Arg1151Trp
XM_005248724.2:c.3439C>T	XP_005248781.1:p.Arg1147Trp
XM_005248726.2:c.3382C>T	XP_005248783.1:p.Arg1128Trp
XM_005248719.4:c.3505C>T	XP_005248776.1:p.Arg1169Trp
XM_005248720.4:c.3478C>T	XP_005248777.1:p.Arg1160Trp
XM_005248721.4:c.3466C>T	XP_005248778.1:p.Arg1156Trp
XM_005248722.4:c.3451C>T	XP_005248779.1:p.Arg1151Trp
XM_005248724.4:c.3439C>T	XP_005248781.1:p.Arg1147Trp
XM_005248726.4:c.3382C>T	XP_005248783.1:p.Arg1128Trp
XM_017010899.2:c.3412C>T	XP_016866388.1:p.Arg1138Trp
XM_024446447.1:c.3505C>T	XP_024302215.1:p.Arg1169Trp
XM_024446448.1:c.3439C>T	XP_024302216.1:p.Arg1147Trp
NM_004999.4:c.3478C>T MANE Select	NP_004990.3:p.Arg1160Trp
NM_001300899.2:c.3409C>T	NP_001287828.1:p.Arg1137Trp
NM_001368136.1:c.3382C>T	NP_001355065.1:p.Arg1128Trp
NM_001368137.1:c.3439C>T	NP_001355066.1:p.Arg1147Trp
NM_001368138.1:c.3394C>T	NP_001355067.1:p.Arg1132Trp
NM_001368865.1:c.3505C>T	NP_001355794.1:p.Arg1169Trp
NM_001368866.1:c.3478C>T	NP_001355795.1:p.Arg1160Trp
NR_160538.1:n.3707C>T