Canonical Allele Identifier: CA364761004

Gene: MYO6

Linked Data

• gnomAD v4: 6-75914065-C-T
• MyVariant Identifiers: chr6:g.76623782C>T (hg19) ; chr6:g.75914065C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914065C>T , CM000668.2:g.75914065C>T	GRCh38
NC_000006.11:g.76623782C>T , CM000668.1:g.76623782C>T	GRCh37
NC_000006.10:g.76680502C>T	NCBI36
NG_009934.1:g.169874C>T
NG_009934.2:g.169873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3346C>T	ENSP00000358992.1:p.Gln1116Ter
ENST00000369977.8:c.3442C>T MANE Select	ENSP00000358994.3:p.Gln1148Ter
ENST00000369985.9:c.3373C>T	ENSP00000359002.3:p.Gln1125Ter
ENST00000664640.1:c.3469C>T	ENSP00000499278.1:p.Gln1157Ter
ENST00000671923.1:c.*1453C>T	ENSP00000500835.1:n.*1453C>T
ENST00000672093.1:c.3442C>T	ENSP00000500710.1:p.Gln1148Ter
ENST00000672162.1:n.1608C>T
ENST00000369975.5:c.3346C>T	ENSP00000358992.1:p.Gln1116Ter
ENST00000369977.7:c.3442C>T	ENSP00000358994.3:p.Gln1148Ter
ENST00000369981.7:c.3472C>T	ENSP00000358998.4:p.Gln1158Ter
ENST00000369985.8:c.3373C>T	ENSP00000359002.3:p.Gln1125Ter
ENST00000615563.4:c.3373C>T	ENSP00000478013.1:p.Gln1125Ter
ENST00000627432.2:c.3469C>T	ENSP00000487348.1:p.Gln1157Ter
NM_001300899.1:c.3373C>T	NP_001287828.1:p.Gln1125Ter
NM_004999.3:c.3442C>T	NP_004990.3:p.Gln1148Ter
XM_005248719.2:c.3469C>T	XP_005248776.1:p.Gln1157Ter
XM_005248720.2:c.3442C>T	XP_005248777.1:p.Gln1148Ter
XM_005248721.2:c.3430C>T	XP_005248778.1:p.Gln1144Ter
XM_005248722.2:c.3415C>T	XP_005248779.1:p.Gln1139Ter
XM_005248724.2:c.3403C>T	XP_005248781.1:p.Gln1135Ter
XM_005248726.2:c.3346C>T	XP_005248783.1:p.Gln1116Ter
XM_005248719.4:c.3469C>T	XP_005248776.1:p.Gln1157Ter
XM_005248720.4:c.3442C>T	XP_005248777.1:p.Gln1148Ter
XM_005248721.4:c.3430C>T	XP_005248778.1:p.Gln1144Ter
XM_005248722.4:c.3415C>T	XP_005248779.1:p.Gln1139Ter
XM_005248724.4:c.3403C>T	XP_005248781.1:p.Gln1135Ter
XM_005248726.4:c.3346C>T	XP_005248783.1:p.Gln1116Ter
XM_017010899.2:c.3376C>T	XP_016866388.1:p.Gln1126Ter
XM_024446447.1:c.3469C>T	XP_024302215.1:p.Gln1157Ter
XM_024446448.1:c.3403C>T	XP_024302216.1:p.Gln1135Ter
NM_004999.4:c.3442C>T MANE Select	NP_004990.3:p.Gln1148Ter
NM_001300899.2:c.3373C>T	NP_001287828.1:p.Gln1125Ter
NM_001368136.1:c.3346C>T	NP_001355065.1:p.Gln1116Ter
NM_001368137.1:c.3403C>T	NP_001355066.1:p.Gln1135Ter
NM_001368138.1:c.3358C>T	NP_001355067.1:p.Gln1120Ter
NM_001368865.1:c.3469C>T	NP_001355794.1:p.Gln1157Ter
NM_001368866.1:c.3442C>T	NP_001355795.1:p.Gln1148Ter
NR_160538.1:n.3671C>T