Canonical Allele Identifier: CA364761963

Gene: MYO6

Linked Data

• MyVariant Identifiers: chr6:g.76623914T>C (hg19) ; chr6:g.75914197T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914197T>C , CM000668.2:g.75914197T>C	GRCh38
NC_000006.11:g.76623914T>C , CM000668.1:g.76623914T>C	GRCh37
NC_000006.10:g.76680634T>C	NCBI36
NG_009934.1:g.170006T>C
NG_009934.2:g.170005T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3478T>C	ENSP00000358992.1:p.Trp1160Arg
ENST00000369977.8:c.3574T>C MANE Select	ENSP00000358994.3:p.Trp1192Arg
ENST00000369985.9:c.3505T>C	ENSP00000359002.3:p.Trp1169Arg
ENST00000664640.1:c.3601T>C	ENSP00000499278.1:p.Trp1201Arg
ENST00000671923.1:c.*1585T>C	ENSP00000500835.1:n.*1585T>C
ENST00000672093.1:c.3574T>C	ENSP00000500710.1:p.Trp1192Arg
ENST00000672162.1:n.1740T>C
ENST00000369975.5:c.3478T>C	ENSP00000358992.1:p.Trp1160Arg
ENST00000369977.7:c.3574T>C	ENSP00000358994.3:p.Trp1192Arg
ENST00000369981.7:c.3604T>C	ENSP00000358998.4:p.Trp1202Arg
ENST00000369985.8:c.3505T>C	ENSP00000359002.3:p.Trp1169Arg
ENST00000615563.4:c.3505T>C	ENSP00000478013.1:p.Trp1169Arg
ENST00000627432.2:c.3601T>C	ENSP00000487348.1:p.Trp1201Arg
NM_001300899.1:c.3505T>C	NP_001287828.1:p.Trp1169Arg
NM_004999.3:c.3574T>C	NP_004990.3:p.Trp1192Arg
XM_005248719.2:c.3601T>C	XP_005248776.1:p.Trp1201Arg
XM_005248720.2:c.3574T>C	XP_005248777.1:p.Trp1192Arg
XM_005248721.2:c.3562T>C	XP_005248778.1:p.Trp1188Arg
XM_005248722.2:c.3547T>C	XP_005248779.1:p.Trp1183Arg
XM_005248724.2:c.3535T>C	XP_005248781.1:p.Trp1179Arg
XM_005248726.2:c.3478T>C	XP_005248783.1:p.Trp1160Arg
XM_005248719.4:c.3601T>C	XP_005248776.1:p.Trp1201Arg
XM_005248720.4:c.3574T>C	XP_005248777.1:p.Trp1192Arg
XM_005248721.4:c.3562T>C	XP_005248778.1:p.Trp1188Arg
XM_005248722.4:c.3547T>C	XP_005248779.1:p.Trp1183Arg
XM_005248724.4:c.3535T>C	XP_005248781.1:p.Trp1179Arg
XM_005248726.4:c.3478T>C	XP_005248783.1:p.Trp1160Arg
XM_017010899.2:c.3508T>C	XP_016866388.1:p.Trp1170Arg
XM_024446447.1:c.3601T>C	XP_024302215.1:p.Trp1201Arg
XM_024446448.1:c.3535T>C	XP_024302216.1:p.Trp1179Arg
NM_004999.4:c.3574T>C MANE Select	NP_004990.3:p.Trp1192Arg
NM_001300899.2:c.3505T>C	NP_001287828.1:p.Trp1169Arg
NM_001368136.1:c.3478T>C	NP_001355065.1:p.Trp1160Arg
NM_001368137.1:c.3535T>C	NP_001355066.1:p.Trp1179Arg
NM_001368138.1:c.3490T>C	NP_001355067.1:p.Trp1164Arg
NM_001368865.1:c.3601T>C	NP_001355794.1:p.Trp1201Arg
NM_001368866.1:c.3574T>C	NP_001355795.1:p.Trp1192Arg
NR_160538.1:n.3803T>C