Canonical Allele Identifier: CA364761155

Gene: MYO6

Linked Data

• gnomAD v4: 6-75914087-T-G
• MyVariant Identifiers: chr6:g.76623804T>G (hg19) ; chr6:g.75914087T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914087T>G , CM000668.2:g.75914087T>G	GRCh38
NC_000006.11:g.76623804T>G , CM000668.1:g.76623804T>G	GRCh37
NC_000006.10:g.76680524T>G	NCBI36
NG_009934.1:g.169896T>G
NG_009934.2:g.169895T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3368T>G	ENSP00000358992.1:p.Ile1123Ser
ENST00000369977.8:c.3464T>G MANE Select	ENSP00000358994.3:p.Ile1155Ser
ENST00000369985.9:c.3395T>G	ENSP00000359002.3:p.Ile1132Ser
ENST00000664640.1:c.3491T>G	ENSP00000499278.1:p.Ile1164Ser
ENST00000671923.1:c.*1475T>G	ENSP00000500835.1:n.*1475T>G
ENST00000672093.1:c.3464T>G	ENSP00000500710.1:p.Ile1155Ser
ENST00000672162.1:n.1630T>G
ENST00000369975.5:c.3368T>G	ENSP00000358992.1:p.Ile1123Ser
ENST00000369977.7:c.3464T>G	ENSP00000358994.3:p.Ile1155Ser
ENST00000369981.7:c.3494T>G	ENSP00000358998.4:p.Ile1165Ser
ENST00000369985.8:c.3395T>G	ENSP00000359002.3:p.Ile1132Ser
ENST00000615563.4:c.3395T>G	ENSP00000478013.1:p.Ile1132Ser
ENST00000627432.2:c.3491T>G	ENSP00000487348.1:p.Ile1164Ser
NM_001300899.1:c.3395T>G	NP_001287828.1:p.Ile1132Ser
NM_004999.3:c.3464T>G	NP_004990.3:p.Ile1155Ser
XM_005248719.2:c.3491T>G	XP_005248776.1:p.Ile1164Ser
XM_005248720.2:c.3464T>G	XP_005248777.1:p.Ile1155Ser
XM_005248721.2:c.3452T>G	XP_005248778.1:p.Ile1151Ser
XM_005248722.2:c.3437T>G	XP_005248779.1:p.Ile1146Ser
XM_005248724.2:c.3425T>G	XP_005248781.1:p.Ile1142Ser
XM_005248726.2:c.3368T>G	XP_005248783.1:p.Ile1123Ser
XM_005248719.4:c.3491T>G	XP_005248776.1:p.Ile1164Ser
XM_005248720.4:c.3464T>G	XP_005248777.1:p.Ile1155Ser
XM_005248721.4:c.3452T>G	XP_005248778.1:p.Ile1151Ser
XM_005248722.4:c.3437T>G	XP_005248779.1:p.Ile1146Ser
XM_005248724.4:c.3425T>G	XP_005248781.1:p.Ile1142Ser
XM_005248726.4:c.3368T>G	XP_005248783.1:p.Ile1123Ser
XM_017010899.2:c.3398T>G	XP_016866388.1:p.Ile1133Ser
XM_024446447.1:c.3491T>G	XP_024302215.1:p.Ile1164Ser
XM_024446448.1:c.3425T>G	XP_024302216.1:p.Ile1142Ser
NM_004999.4:c.3464T>G MANE Select	NP_004990.3:p.Ile1155Ser
NM_001300899.2:c.3395T>G	NP_001287828.1:p.Ile1132Ser
NM_001368136.1:c.3368T>G	NP_001355065.1:p.Ile1123Ser
NM_001368137.1:c.3425T>G	NP_001355066.1:p.Ile1142Ser
NM_001368138.1:c.3380T>G	NP_001355067.1:p.Ile1127Ser
NM_001368865.1:c.3491T>G	NP_001355794.1:p.Ile1164Ser
NM_001368866.1:c.3464T>G	NP_001355795.1:p.Ile1155Ser
NR_160538.1:n.3693T>G