Canonical Allele Identifier: CA364762352

Gene: MYO6

Linked Data

• MyVariant Identifiers: chr6:g.76623967T>G (hg19) ; chr6:g.75914250T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914250T>G , CM000668.2:g.75914250T>G	GRCh38
NC_000006.11:g.76623967T>G , CM000668.1:g.76623967T>G	GRCh37
NC_000006.10:g.76680687T>G	NCBI36
NG_009934.1:g.170059T>G
NG_009934.2:g.170058T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3531T>G	ENSP00000358992.1:p.His1177Gln
ENST00000369977.8:c.3627T>G MANE Select	ENSP00000358994.3:p.His1209Gln
ENST00000369985.9:c.3558T>G	ENSP00000359002.3:p.His1186Gln
ENST00000664640.1:c.3654T>G	ENSP00000499278.1:p.His1218Gln
ENST00000671923.1:c.*1638T>G	ENSP00000500835.1:n.*1638T>G
ENST00000672093.1:c.3627T>G	ENSP00000500710.1:p.His1209Gln
ENST00000672162.1:n.1793T>G
ENST00000369975.5:c.3531T>G	ENSP00000358992.1:p.His1177Gln
ENST00000369977.7:c.3627T>G	ENSP00000358994.3:p.His1209Gln
ENST00000369981.7:c.3657T>G	ENSP00000358998.4:p.His1219Gln
ENST00000369985.8:c.3558T>G	ENSP00000359002.3:p.His1186Gln
ENST00000615563.4:c.3558T>G	ENSP00000478013.1:p.His1186Gln
ENST00000627432.2:c.3654T>G	ENSP00000487348.1:p.His1218Gln
NM_001300899.1:c.3558T>G	NP_001287828.1:p.His1186Gln
NM_004999.3:c.3627T>G	NP_004990.3:p.His1209Gln
XM_005248719.2:c.3654T>G	XP_005248776.1:p.His1218Gln
XM_005248720.2:c.3627T>G	XP_005248777.1:p.His1209Gln
XM_005248721.2:c.3615T>G	XP_005248778.1:p.His1205Gln
XM_005248722.2:c.3600T>G	XP_005248779.1:p.His1200Gln
XM_005248724.2:c.3588T>G	XP_005248781.1:p.His1196Gln
XM_005248726.2:c.3531T>G	XP_005248783.1:p.His1177Gln
XM_005248719.4:c.3654T>G	XP_005248776.1:p.His1218Gln
XM_005248720.4:c.3627T>G	XP_005248777.1:p.His1209Gln
XM_005248721.4:c.3615T>G	XP_005248778.1:p.His1205Gln
XM_005248722.4:c.3600T>G	XP_005248779.1:p.His1200Gln
XM_005248724.4:c.3588T>G	XP_005248781.1:p.His1196Gln
XM_005248726.4:c.3531T>G	XP_005248783.1:p.His1177Gln
XM_017010899.2:c.3561T>G	XP_016866388.1:p.His1187Gln
XM_024446447.1:c.3654T>G	XP_024302215.1:p.His1218Gln
XM_024446448.1:c.3588T>G	XP_024302216.1:p.His1196Gln
NM_004999.4:c.3627T>G MANE Select	NP_004990.3:p.His1209Gln
NM_001300899.2:c.3558T>G	NP_001287828.1:p.His1186Gln
NM_001368136.1:c.3531T>G	NP_001355065.1:p.His1177Gln
NM_001368137.1:c.3588T>G	NP_001355066.1:p.His1196Gln
NM_001368138.1:c.3543T>G	NP_001355067.1:p.His1181Gln
NM_001368865.1:c.3654T>G	NP_001355794.1:p.His1218Gln
NM_001368866.1:c.3627T>G	NP_001355795.1:p.His1209Gln
NR_160538.1:n.3856T>G