Canonical Allele Identifier: CA3897730

Gene: MYO6

Linked Data

• dbSNP Id: rs376848570
• ExAC: 6:76623751 G / A
• gnomAD v2: 6-76623751-G-A
• gnomAD v3: 6-75914034-G-A
• gnomAD v4: 6-75914034-G-A
• MyVariant Identifiers: chr6:g.76623751G>A (hg19) ; chr6:g.75914034G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914034G>A , CM000668.2:g.75914034G>A	GRCh38
NC_000006.11:g.76623751G>A , CM000668.1:g.76623751G>A	GRCh37
NC_000006.10:g.76680471G>A	NCBI36
NG_009934.1:g.169843G>A
NG_009934.2:g.169842G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369975.6:c.3344-29G>A	ENSP00000358992.1:n.3344-29G>A
ENST00000369977.8:c.3440-29G>A MANE Select	ENSP00000358994.3:n.3440-29G>A
ENST00000369985.9:c.3371-29G>A	ENSP00000359002.3:n.3371-29G>A
ENST00000664640.1:c.3467-29G>A	ENSP00000499278.1:n.3467-29G>A
ENST00000671923.1:c.*1451-29G>A	ENSP00000500835.1:n.*1451-29G>A
ENST00000672093.1:c.3440-29G>A	ENSP00000500710.1:n.3440-29G>A
ENST00000672162.1:n.1606-29G>A
ENST00000369975.5:c.3344-29G>A	ENSP00000358992.1:n.3344-29G>A
ENST00000369977.7:c.3440-29G>A	ENSP00000358994.3:n.3440-29G>A
ENST00000369981.7:c.3470-29G>A	ENSP00000358998.4:n.3470-29G>A
ENST00000369985.8:c.3371-29G>A	ENSP00000359002.3:n.3371-29G>A
ENST00000615563.4:c.3371-29G>A	ENSP00000478013.1:n.3371-29G>A
ENST00000627432.2:c.3467-29G>A	ENSP00000487348.1:n.3467-29G>A
NM_001300899.1:c.3371-29G>A	NP_001287828.1:n.3371-29G>A
NM_004999.3:c.3440-29G>A	NP_004990.3:n.3440-29G>A
XM_005248719.2:c.3467-29G>A	XP_005248776.1:n.3467-29G>A
XM_005248720.2:c.3440-29G>A	XP_005248777.1:n.3440-29G>A
XM_005248721.2:c.3428-29G>A	XP_005248778.1:n.3428-29G>A
XM_005248722.2:c.3413-29G>A	XP_005248779.1:n.3413-29G>A
XM_005248724.2:c.3401-29G>A	XP_005248781.1:n.3401-29G>A
XM_005248726.2:c.3344-29G>A	XP_005248783.1:n.3344-29G>A
XM_005248719.4:c.3467-29G>A	XP_005248776.1:n.3467-29G>A
XM_005248720.4:c.3440-29G>A	XP_005248777.1:n.3440-29G>A
XM_005248721.4:c.3428-29G>A	XP_005248778.1:n.3428-29G>A
XM_005248722.4:c.3413-29G>A	XP_005248779.1:n.3413-29G>A
XM_005248724.4:c.3401-29G>A	XP_005248781.1:n.3401-29G>A
XM_005248726.4:c.3344-29G>A	XP_005248783.1:n.3344-29G>A
XM_017010899.2:c.3374-29G>A	XP_016866388.1:n.3374-29G>A
XM_024446447.1:c.3467-29G>A	XP_024302215.1:n.3467-29G>A
XM_024446448.1:c.3401-29G>A	XP_024302216.1:n.3401-29G>A
NM_004999.4:c.3440-29G>A MANE Select	NP_004990.3:n.3440-29G>A
NM_001300899.2:c.3371-29G>A	NP_001287828.1:n.3371-29G>A
NM_001368136.1:c.3344-29G>A	NP_001355065.1:n.3344-29G>A
NM_001368137.1:c.3401-29G>A	NP_001355066.1:n.3401-29G>A
NM_001368138.1:c.3356-29G>A	NP_001355067.1:n.3356-29G>A
NM_001368865.1:c.3467-29G>A	NP_001355794.1:n.3467-29G>A
NM_001368866.1:c.3440-29G>A	NP_001355795.1:n.3440-29G>A
NR_160538.1:n.3669-29G>A