Canonical Allele Identifier: CA2771759992

Gene: MYO6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914072_75914073insAGTTAT , CM000668.2:g.75914072_75914073insAGTTAT	GRCh38
NC_000006.11:g.76623789_76623790insAGTTAT , CM000668.1:g.76623789_76623790insAGTTAT	GRCh37
NC_000006.10:g.76680509_76680510insAGTTAT	NCBI36
NG_009934.1:g.169881_169882insAGTTAT
NG_009934.2:g.169880_169881insAGTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3353_3354insAGTTAT	ENSP00000358992.1:p.Asn1118delinsLysValIle
ENST00000369977.8:c.3449_3450insAGTTAT MANE Select	ENSP00000358994.3:p.Asn1150delinsLysValIle
ENST00000369985.9:c.3380_3381insAGTTAT	ENSP00000359002.3:p.Asn1127delinsLysValIle
ENST00000664640.1:c.3476_3477insAGTTAT	ENSP00000499278.1:p.Asn1159delinsLysValIle
ENST00000671923.1:c.*1460_*1461insAGTTAT	ENSP00000500835.1:n.*1460_*1461insAGTTAT
ENST00000672093.1:c.3449_3450insAGTTAT	ENSP00000500710.1:p.Asn1150delinsLysValIle
ENST00000672162.1:n.1615_1616insAGTTAT
ENST00000369975.5:c.3353_3354insAGTTAT	ENSP00000358992.1:p.Asn1118delinsLysValIle
ENST00000369977.7:c.3449_3450insAGTTAT	ENSP00000358994.3:p.Asn1150delinsLysValIle
ENST00000369981.7:c.3479_3480insAGTTAT	ENSP00000358998.4:p.Asn1160delinsLysValIle
ENST00000369985.8:c.3380_3381insAGTTAT	ENSP00000359002.3:p.Asn1127delinsLysValIle
ENST00000615563.4:c.3380_3381insAGTTAT	ENSP00000478013.1:p.Asn1127delinsLysValIle
ENST00000627432.2:c.3476_3477insAGTTAT	ENSP00000487348.1:p.Asn1159delinsLysValIle
NM_001300899.1:c.3380_3381insAGTTAT	NP_001287828.1:p.Asn1127delinsLysValIle
NM_004999.3:c.3449_3450insAGTTAT	NP_004990.3:p.Asn1150delinsLysValIle
XM_005248719.2:c.3476_3477insAGTTAT	XP_005248776.1:p.Asn1159delinsLysValIle
XM_005248720.2:c.3449_3450insAGTTAT	XP_005248777.1:p.Asn1150delinsLysValIle
XM_005248721.2:c.3437_3438insAGTTAT	XP_005248778.1:p.Asn1146delinsLysValIle
XM_005248722.2:c.3422_3423insAGTTAT	XP_005248779.1:p.Asn1141delinsLysValIle
XM_005248724.2:c.3410_3411insAGTTAT	XP_005248781.1:p.Asn1137delinsLysValIle
XM_005248726.2:c.3353_3354insAGTTAT	XP_005248783.1:p.Asn1118delinsLysValIle
XM_005248719.4:c.3476_3477insAGTTAT	XP_005248776.1:p.Asn1159delinsLysValIle
XM_005248720.4:c.3449_3450insAGTTAT	XP_005248777.1:p.Asn1150delinsLysValIle
XM_005248721.4:c.3437_3438insAGTTAT	XP_005248778.1:p.Asn1146delinsLysValIle
XM_005248722.4:c.3422_3423insAGTTAT	XP_005248779.1:p.Asn1141delinsLysValIle
XM_005248724.4:c.3410_3411insAGTTAT	XP_005248781.1:p.Asn1137delinsLysValIle
XM_005248726.4:c.3353_3354insAGTTAT	XP_005248783.1:p.Asn1118delinsLysValIle
XM_017010899.2:c.3383_3384insAGTTAT	XP_016866388.1:p.Asn1128delinsLysValIle
XM_024446447.1:c.3476_3477insAGTTAT	XP_024302215.1:p.Asn1159delinsLysValIle
XM_024446448.1:c.3410_3411insAGTTAT	XP_024302216.1:p.Asn1137delinsLysValIle
NM_004999.4:c.3449_3450insAGTTAT MANE Select	NP_004990.3:p.Asn1150delinsLysValIle
NM_001300899.2:c.3380_3381insAGTTAT	NP_001287828.1:p.Asn1127delinsLysValIle
NM_001368136.1:c.3353_3354insAGTTAT	NP_001355065.1:p.Asn1118delinsLysValIle
NM_001368137.1:c.3410_3411insAGTTAT	NP_001355066.1:p.Asn1137delinsLysValIle
NM_001368138.1:c.3365_3366insAGTTAT	NP_001355067.1:p.Asn1122delinsLysValIle
NM_001368865.1:c.3476_3477insAGTTAT	NP_001355794.1:p.Asn1159delinsLysValIle
NM_001368866.1:c.3449_3450insAGTTAT	NP_001355795.1:p.Asn1150delinsLysValIle
NR_160538.1:n.3678_3679insAGTTAT