Canonical Allele Identifier: CA364762211

Gene: MYO6

Linked Data

• MyVariant Identifiers: chr6:g.76623945T>A (hg19) ; chr6:g.75914228T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914228T>A , CM000668.2:g.75914228T>A	GRCh38
NC_000006.11:g.76623945T>A , CM000668.1:g.76623945T>A	GRCh37
NC_000006.10:g.76680665T>A	NCBI36
NG_009934.1:g.170037T>A
NG_009934.2:g.170036T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3509T>A	ENSP00000358992.1:p.Ile1170Asn
ENST00000369977.8:c.3605T>A MANE Select	ENSP00000358994.3:p.Ile1202Asn
ENST00000369985.9:c.3536T>A	ENSP00000359002.3:p.Ile1179Asn
ENST00000664640.1:c.3632T>A	ENSP00000499278.1:p.Ile1211Asn
ENST00000671923.1:c.*1616T>A	ENSP00000500835.1:n.*1616T>A
ENST00000672093.1:c.3605T>A	ENSP00000500710.1:p.Ile1202Asn
ENST00000672162.1:n.1771T>A
ENST00000369975.5:c.3509T>A	ENSP00000358992.1:p.Ile1170Asn
ENST00000369977.7:c.3605T>A	ENSP00000358994.3:p.Ile1202Asn
ENST00000369981.7:c.3635T>A	ENSP00000358998.4:p.Ile1212Asn
ENST00000369985.8:c.3536T>A	ENSP00000359002.3:p.Ile1179Asn
ENST00000615563.4:c.3536T>A	ENSP00000478013.1:p.Ile1179Asn
ENST00000627432.2:c.3632T>A	ENSP00000487348.1:p.Ile1211Asn
NM_001300899.1:c.3536T>A	NP_001287828.1:p.Ile1179Asn
NM_004999.3:c.3605T>A	NP_004990.3:p.Ile1202Asn
XM_005248719.2:c.3632T>A	XP_005248776.1:p.Ile1211Asn
XM_005248720.2:c.3605T>A	XP_005248777.1:p.Ile1202Asn
XM_005248721.2:c.3593T>A	XP_005248778.1:p.Ile1198Asn
XM_005248722.2:c.3578T>A	XP_005248779.1:p.Ile1193Asn
XM_005248724.2:c.3566T>A	XP_005248781.1:p.Ile1189Asn
XM_005248726.2:c.3509T>A	XP_005248783.1:p.Ile1170Asn
XM_005248719.4:c.3632T>A	XP_005248776.1:p.Ile1211Asn
XM_005248720.4:c.3605T>A	XP_005248777.1:p.Ile1202Asn
XM_005248721.4:c.3593T>A	XP_005248778.1:p.Ile1198Asn
XM_005248722.4:c.3578T>A	XP_005248779.1:p.Ile1193Asn
XM_005248724.4:c.3566T>A	XP_005248781.1:p.Ile1189Asn
XM_005248726.4:c.3509T>A	XP_005248783.1:p.Ile1170Asn
XM_017010899.2:c.3539T>A	XP_016866388.1:p.Ile1180Asn
XM_024446447.1:c.3632T>A	XP_024302215.1:p.Ile1211Asn
XM_024446448.1:c.3566T>A	XP_024302216.1:p.Ile1189Asn
NM_004999.4:c.3605T>A MANE Select	NP_004990.3:p.Ile1202Asn
NM_001300899.2:c.3536T>A	NP_001287828.1:p.Ile1179Asn
NM_001368136.1:c.3509T>A	NP_001355065.1:p.Ile1170Asn
NM_001368137.1:c.3566T>A	NP_001355066.1:p.Ile1189Asn
NM_001368138.1:c.3521T>A	NP_001355067.1:p.Ile1174Asn
NM_001368865.1:c.3632T>A	NP_001355794.1:p.Ile1211Asn
NM_001368866.1:c.3605T>A	NP_001355795.1:p.Ile1202Asn
NR_160538.1:n.3834T>A