Canonical Allele Identifier: CA2771759986

Gene: MYO6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914070_75914071insGG , CM000668.2:g.75914070_75914071insGG	GRCh38
NC_000006.11:g.76623787_76623788insGG , CM000668.1:g.76623787_76623788insGG	GRCh37
NC_000006.10:g.76680507_76680508insGG	NCBI36
NG_009934.1:g.169879_169880insGG
NG_009934.2:g.169878_169879insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3351_3352insGG	ENSP00000358992.1:p.Asn1118GlyfsTer16
ENST00000369977.8:c.3447_3448insGG MANE Select	ENSP00000358994.3:p.Asn1150GlyfsTer16
ENST00000369985.9:c.3378_3379insGG	ENSP00000359002.3:p.Asn1127GlyfsTer16
ENST00000664640.1:c.3474_3475insGG	ENSP00000499278.1:p.Asn1159GlyfsTer16
ENST00000671923.1:c.*1458_*1459insGG	ENSP00000500835.1:n.*1458_*1459insGG
ENST00000672093.1:c.3447_3448insGG	ENSP00000500710.1:p.Asn1150GlyfsTer16
ENST00000672162.1:n.1613_1614insGG
ENST00000369975.5:c.3351_3352insGG	ENSP00000358992.1:p.Asn1118GlyfsTer16
ENST00000369977.7:c.3447_3448insGG	ENSP00000358994.3:p.Asn1150GlyfsTer16
ENST00000369981.7:c.3477_3478insGG	ENSP00000358998.4:p.Asn1160GlyfsTer16
ENST00000369985.8:c.3378_3379insGG	ENSP00000359002.3:p.Asn1127GlyfsTer16
ENST00000615563.4:c.3378_3379insGG	ENSP00000478013.1:p.Asn1127GlyfsTer16
ENST00000627432.2:c.3474_3475insGG	ENSP00000487348.1:p.Asn1159GlyfsTer16
NM_001300899.1:c.3378_3379insGG	NP_001287828.1:p.Asn1127GlyfsTer16
NM_004999.3:c.3447_3448insGG	NP_004990.3:p.Asn1150GlyfsTer16
XM_005248719.2:c.3474_3475insGG	XP_005248776.1:p.Asn1159GlyfsTer16
XM_005248720.2:c.3447_3448insGG	XP_005248777.1:p.Asn1150GlyfsTer16
XM_005248721.2:c.3435_3436insGG	XP_005248778.1:p.Asn1146GlyfsTer16
XM_005248722.2:c.3420_3421insGG	XP_005248779.1:p.Asn1141GlyfsTer16
XM_005248724.2:c.3408_3409insGG	XP_005248781.1:p.Asn1137GlyfsTer16
XM_005248726.2:c.3351_3352insGG	XP_005248783.1:p.Asn1118GlyfsTer16
XM_005248719.4:c.3474_3475insGG	XP_005248776.1:p.Asn1159GlyfsTer16
XM_005248720.4:c.3447_3448insGG	XP_005248777.1:p.Asn1150GlyfsTer16
XM_005248721.4:c.3435_3436insGG	XP_005248778.1:p.Asn1146GlyfsTer16
XM_005248722.4:c.3420_3421insGG	XP_005248779.1:p.Asn1141GlyfsTer16
XM_005248724.4:c.3408_3409insGG	XP_005248781.1:p.Asn1137GlyfsTer16
XM_005248726.4:c.3351_3352insGG	XP_005248783.1:p.Asn1118GlyfsTer16
XM_017010899.2:c.3381_3382insGG	XP_016866388.1:p.Asn1128GlyfsTer16
XM_024446447.1:c.3474_3475insGG	XP_024302215.1:p.Asn1159GlyfsTer16
XM_024446448.1:c.3408_3409insGG	XP_024302216.1:p.Asn1137GlyfsTer16
NM_004999.4:c.3447_3448insGG MANE Select	NP_004990.3:p.Asn1150GlyfsTer16
NM_001300899.2:c.3378_3379insGG	NP_001287828.1:p.Asn1127GlyfsTer16
NM_001368136.1:c.3351_3352insGG	NP_001355065.1:p.Asn1118GlyfsTer16
NM_001368137.1:c.3408_3409insGG	NP_001355066.1:p.Asn1137GlyfsTer16
NM_001368138.1:c.3363_3364insGG	NP_001355067.1:p.Asn1122GlyfsTer16
NM_001368865.1:c.3474_3475insGG	NP_001355794.1:p.Asn1159GlyfsTer16
NM_001368866.1:c.3447_3448insGG	NP_001355795.1:p.Asn1150GlyfsTer16
NR_160538.1:n.3676_3677insGG