Canonical Allele Identifier: CA364761953

Gene: MYO6

Linked Data

• MyVariant Identifiers: chr6:g.76623911G>T (hg19) ; chr6:g.75914194G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914194G>T , CM000668.2:g.75914194G>T	GRCh38
NC_000006.11:g.76623911G>T , CM000668.1:g.76623911G>T	GRCh37
NC_000006.10:g.76680631G>T	NCBI36
NG_009934.1:g.170003G>T
NG_009934.2:g.170002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3475G>T	ENSP00000358992.1:p.Gly1159Cys
ENST00000369977.8:c.3571G>T MANE Select	ENSP00000358994.3:p.Gly1191Cys
ENST00000369985.9:c.3502G>T	ENSP00000359002.3:p.Gly1168Cys
ENST00000664640.1:c.3598G>T	ENSP00000499278.1:p.Gly1200Cys
ENST00000671923.1:c.*1582G>T	ENSP00000500835.1:n.*1582G>T
ENST00000672093.1:c.3571G>T	ENSP00000500710.1:p.Gly1191Cys
ENST00000672162.1:n.1737G>T
ENST00000369975.5:c.3475G>T	ENSP00000358992.1:p.Gly1159Cys
ENST00000369977.7:c.3571G>T	ENSP00000358994.3:p.Gly1191Cys
ENST00000369981.7:c.3601G>T	ENSP00000358998.4:p.Gly1201Cys
ENST00000369985.8:c.3502G>T	ENSP00000359002.3:p.Gly1168Cys
ENST00000615563.4:c.3502G>T	ENSP00000478013.1:p.Gly1168Cys
ENST00000627432.2:c.3598G>T	ENSP00000487348.1:p.Gly1200Cys
NM_001300899.1:c.3502G>T	NP_001287828.1:p.Gly1168Cys
NM_004999.3:c.3571G>T	NP_004990.3:p.Gly1191Cys
XM_005248719.2:c.3598G>T	XP_005248776.1:p.Gly1200Cys
XM_005248720.2:c.3571G>T	XP_005248777.1:p.Gly1191Cys
XM_005248721.2:c.3559G>T	XP_005248778.1:p.Gly1187Cys
XM_005248722.2:c.3544G>T	XP_005248779.1:p.Gly1182Cys
XM_005248724.2:c.3532G>T	XP_005248781.1:p.Gly1178Cys
XM_005248726.2:c.3475G>T	XP_005248783.1:p.Gly1159Cys
XM_005248719.4:c.3598G>T	XP_005248776.1:p.Gly1200Cys
XM_005248720.4:c.3571G>T	XP_005248777.1:p.Gly1191Cys
XM_005248721.4:c.3559G>T	XP_005248778.1:p.Gly1187Cys
XM_005248722.4:c.3544G>T	XP_005248779.1:p.Gly1182Cys
XM_005248724.4:c.3532G>T	XP_005248781.1:p.Gly1178Cys
XM_005248726.4:c.3475G>T	XP_005248783.1:p.Gly1159Cys
XM_017010899.2:c.3505G>T	XP_016866388.1:p.Gly1169Cys
XM_024446447.1:c.3598G>T	XP_024302215.1:p.Gly1200Cys
XM_024446448.1:c.3532G>T	XP_024302216.1:p.Gly1178Cys
NM_004999.4:c.3571G>T MANE Select	NP_004990.3:p.Gly1191Cys
NM_001300899.2:c.3502G>T	NP_001287828.1:p.Gly1168Cys
NM_001368136.1:c.3475G>T	NP_001355065.1:p.Gly1159Cys
NM_001368137.1:c.3532G>T	NP_001355066.1:p.Gly1178Cys
NM_001368138.1:c.3487G>T	NP_001355067.1:p.Gly1163Cys
NM_001368865.1:c.3598G>T	NP_001355794.1:p.Gly1200Cys
NM_001368866.1:c.3571G>T	NP_001355795.1:p.Gly1191Cys
NR_160538.1:n.3800G>T