Canonical Allele Identifier: CA450938564

Gene: MYO6

Linked Data

• dbSNP Id: rs1311361356
• MyVariant Identifiers: chr6:g.76623961A>G (hg19) ; chr6:g.75914244A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914244A>G , CM000668.2:g.75914244A>G	GRCh38
NC_000006.11:g.76623961A>G , CM000668.1:g.76623961A>G	GRCh37
NC_000006.10:g.76680681A>G	NCBI36
NG_009934.1:g.170053A>G
NG_009934.2:g.170052A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3525A>G	ENSP00000358992.1:p.Glu1175=
ENST00000369977.8:c.3621A>G MANE Select	ENSP00000358994.3:p.Glu1207=
ENST00000369985.9:c.3552A>G	ENSP00000359002.3:p.Glu1184=
ENST00000664640.1:c.3648A>G	ENSP00000499278.1:p.Glu1216=
ENST00000671923.1:c.*1632A>G	ENSP00000500835.1:n.*1632A>G
ENST00000672093.1:c.3621A>G	ENSP00000500710.1:p.Glu1207=
ENST00000672162.1:n.1787A>G
ENST00000369975.5:c.3525A>G	ENSP00000358992.1:p.Glu1175=
ENST00000369977.7:c.3621A>G	ENSP00000358994.3:p.Glu1207=
ENST00000369981.7:c.3651A>G	ENSP00000358998.4:p.Glu1217=
ENST00000369985.8:c.3552A>G	ENSP00000359002.3:p.Glu1184=
ENST00000615563.4:c.3552A>G	ENSP00000478013.1:p.Glu1184=
ENST00000627432.2:c.3648A>G	ENSP00000487348.1:p.Glu1216=
NM_001300899.1:c.3552A>G	NP_001287828.1:p.Glu1184=
NM_004999.3:c.3621A>G	NP_004990.3:p.Glu1207=
XM_005248719.2:c.3648A>G	XP_005248776.1:p.Glu1216=
XM_005248720.2:c.3621A>G	XP_005248777.1:p.Glu1207=
XM_005248721.2:c.3609A>G	XP_005248778.1:p.Glu1203=
XM_005248722.2:c.3594A>G	XP_005248779.1:p.Glu1198=
XM_005248724.2:c.3582A>G	XP_005248781.1:p.Glu1194=
XM_005248726.2:c.3525A>G	XP_005248783.1:p.Glu1175=
XM_005248719.4:c.3648A>G	XP_005248776.1:p.Glu1216=
XM_005248720.4:c.3621A>G	XP_005248777.1:p.Glu1207=
XM_005248721.4:c.3609A>G	XP_005248778.1:p.Glu1203=
XM_005248722.4:c.3594A>G	XP_005248779.1:p.Glu1198=
XM_005248724.4:c.3582A>G	XP_005248781.1:p.Glu1194=
XM_005248726.4:c.3525A>G	XP_005248783.1:p.Glu1175=
XM_017010899.2:c.3555A>G	XP_016866388.1:p.Glu1185=
XM_024446447.1:c.3648A>G	XP_024302215.1:p.Glu1216=
XM_024446448.1:c.3582A>G	XP_024302216.1:p.Glu1194=
NM_004999.4:c.3621A>G MANE Select	NP_004990.3:p.Glu1207=
NM_001300899.2:c.3552A>G	NP_001287828.1:p.Glu1184=
NM_001368136.1:c.3525A>G	NP_001355065.1:p.Glu1175=
NM_001368137.1:c.3582A>G	NP_001355066.1:p.Glu1194=
NM_001368138.1:c.3537A>G	NP_001355067.1:p.Glu1179=
NM_001368865.1:c.3648A>G	NP_001355794.1:p.Glu1216=
NM_001368866.1:c.3621A>G	NP_001355795.1:p.Glu1207=
NR_160538.1:n.3850A>G