Canonical Allele Identifier: CA2771760955

Gene: MYO6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75919063G>C , CM000668.2:g.75919063G>C	GRCh38
NC_000006.11:g.76628780G>C , CM000668.1:g.76628780G>C	GRCh37
NC_000006.10:g.76685500G>C	NCBI36
NG_009934.1:g.174872G>C
NG_009934.2:g.174871G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369977.8:c.*4051G>C MANE Select	ENSP00000358994.3:n.*4051G>C
ENST00000369985.9:c.*4051G>C	ENSP00000359002.3:n.*4051G>C
ENST00000664640.1:c.*4051G>C	ENSP00000499278.1:n.*4051G>C
ENST00000369981.7:c.*4051G>C	ENSP00000358998.4:n.*4051G>C
ENST00000369985.8:c.*4051G>C	ENSP00000359002.3:n.*4051G>C
NM_001300899.1:c.*4051G>C	NP_001287828.1:n.*4051G>C
NM_004999.3:c.*4051G>C	NP_004990.3:n.*4051G>C
XM_005248719.4:c.*4051G>C	XP_005248776.1:n.*4051G>C
XM_005248720.4:c.*4051G>C	XP_005248777.1:n.*4051G>C
XM_005248721.4:c.*4051G>C	XP_005248778.1:n.*4051G>C
XM_005248722.4:c.*4051G>C	XP_005248779.1:n.*4051G>C
XM_005248724.4:c.*4051G>C	XP_005248781.1:n.*4051G>C
XM_005248726.4:c.*4051G>C	XP_005248783.1:n.*4051G>C
XM_017010899.2:c.*4051G>C	XP_016866388.1:n.*4051G>C
XM_024446447.1:c.*4051G>C	XP_024302215.1:n.*4051G>C
XM_024446448.1:c.*4051G>C	XP_024302216.1:n.*4051G>C
NM_004999.4:c.*4051G>C MANE Select	NP_004990.3:n.*4051G>C
NM_001300899.2:c.*4051G>C	NP_001287828.1:n.*4051G>C
NM_001368136.1:c.*4051G>C	NP_001355065.1:n.*4051G>C
NM_001368137.1:c.*4051G>C	NP_001355066.1:n.*4051G>C
NM_001368138.1:c.*4051G>C	NP_001355067.1:n.*4051G>C
NM_001368865.1:c.*4051G>C	NP_001355794.1:n.*4051G>C
NM_001368866.1:c.*4051G>C	NP_001355795.1:n.*4051G>C
NR_160538.1:n.8138G>C