Canonical Allele Identifier: CA2679455935

Gene: MYO6

Linked Data

• gnomAD v4: 6-75913975-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75913975_75913976insCAG , CM000668.2:g.75913975_75913976insCAG	GRCh38
NC_000006.11:g.76623692_76623693insCAG , CM000668.1:g.76623692_76623693insCAG	GRCh37
NC_000006.10:g.76680412_76680413insCAG	NCBI36
NG_009934.1:g.169784_169785insCAG
NG_009934.2:g.169783_169784insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3344-88_3344-87insCAG	ENSP00000358992.1:n.3344-88_3344-87insCAG
ENST00000369977.8:c.3440-88_3440-87insCAG MANE Select	ENSP00000358994.3:n.3440-88_3440-87insCAG
ENST00000369985.9:c.3371-88_3371-87insCAG	ENSP00000359002.3:n.3371-88_3371-87insCAG
ENST00000664640.1:c.3467-88_3467-87insCAG	ENSP00000499278.1:n.3467-88_3467-87insCAG
ENST00000671923.1:c.*1451-88_*1451-87insCAG	ENSP00000500835.1:n.*1451-88_*1451-87insCAG
ENST00000672093.1:c.3440-88_3440-87insCAG	ENSP00000500710.1:n.3440-88_3440-87insCAG
ENST00000672162.1:n.1606-88_1606-87insCAG
ENST00000369975.5:c.3344-88_3344-87insCAG	ENSP00000358992.1:n.3344-88_3344-87insCAG
ENST00000369977.7:c.3440-88_3440-87insCAG	ENSP00000358994.3:n.3440-88_3440-87insCAG
ENST00000369981.7:c.3470-88_3470-87insCAG	ENSP00000358998.4:n.3470-88_3470-87insCAG
ENST00000369985.8:c.3371-88_3371-87insCAG	ENSP00000359002.3:n.3371-88_3371-87insCAG
ENST00000615563.4:c.3371-88_3371-87insCAG	ENSP00000478013.1:n.3371-88_3371-87insCAG
ENST00000627432.2:c.3467-88_3467-87insCAG	ENSP00000487348.1:n.3467-88_3467-87insCAG
NM_001300899.1:c.3371-88_3371-87insCAG	NP_001287828.1:n.3371-88_3371-87insCAG
NM_004999.3:c.3440-88_3440-87insCAG	NP_004990.3:n.3440-88_3440-87insCAG
XM_005248719.2:c.3467-88_3467-87insCAG	XP_005248776.1:n.3467-88_3467-87insCAG
XM_005248720.2:c.3440-88_3440-87insCAG	XP_005248777.1:n.3440-88_3440-87insCAG
XM_005248721.2:c.3428-88_3428-87insCAG	XP_005248778.1:n.3428-88_3428-87insCAG
XM_005248722.2:c.3413-88_3413-87insCAG	XP_005248779.1:n.3413-88_3413-87insCAG
XM_005248724.2:c.3401-88_3401-87insCAG	XP_005248781.1:n.3401-88_3401-87insCAG
XM_005248726.2:c.3344-88_3344-87insCAG	XP_005248783.1:n.3344-88_3344-87insCAG
XM_005248719.4:c.3467-88_3467-87insCAG	XP_005248776.1:n.3467-88_3467-87insCAG
XM_005248720.4:c.3440-88_3440-87insCAG	XP_005248777.1:n.3440-88_3440-87insCAG
XM_005248721.4:c.3428-88_3428-87insCAG	XP_005248778.1:n.3428-88_3428-87insCAG
XM_005248722.4:c.3413-88_3413-87insCAG	XP_005248779.1:n.3413-88_3413-87insCAG
XM_005248724.4:c.3401-88_3401-87insCAG	XP_005248781.1:n.3401-88_3401-87insCAG
XM_005248726.4:c.3344-88_3344-87insCAG	XP_005248783.1:n.3344-88_3344-87insCAG
XM_017010899.2:c.3374-88_3374-87insCAG	XP_016866388.1:n.3374-88_3374-87insCAG
XM_024446447.1:c.3467-88_3467-87insCAG	XP_024302215.1:n.3467-88_3467-87insCAG
XM_024446448.1:c.3401-88_3401-87insCAG	XP_024302216.1:n.3401-88_3401-87insCAG
NM_004999.4:c.3440-88_3440-87insCAG MANE Select	NP_004990.3:n.3440-88_3440-87insCAG
NM_001300899.2:c.3371-88_3371-87insCAG	NP_001287828.1:n.3371-88_3371-87insCAG
NM_001368136.1:c.3344-88_3344-87insCAG	NP_001355065.1:n.3344-88_3344-87insCAG
NM_001368137.1:c.3401-88_3401-87insCAG	NP_001355066.1:n.3401-88_3401-87insCAG
NM_001368138.1:c.3356-88_3356-87insCAG	NP_001355067.1:n.3356-88_3356-87insCAG
NM_001368865.1:c.3467-88_3467-87insCAG	NP_001355794.1:n.3467-88_3467-87insCAG
NM_001368866.1:c.3440-88_3440-87insCAG	NP_001355795.1:n.3440-88_3440-87insCAG
NR_160538.1:n.3669-88_3669-87insCAG