Canonical Allele Identifier: CA364761036

Gene: MYO6

Linked Data

• dbSNP Id: rs1780971090
• MyVariant Identifiers: chr6:g.76623789A>C (hg19) ; chr6:g.75914072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75914072A>C , CM000668.2:g.75914072A>C	GRCh38
NC_000006.11:g.76623789A>C , CM000668.1:g.76623789A>C	GRCh37
NC_000006.10:g.76680509A>C	NCBI36
NG_009934.1:g.169881A>C
NG_009934.2:g.169880A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369975.6:c.3353A>C	ENSP00000358992.1:p.Asn1118Thr
ENST00000369977.8:c.3449A>C MANE Select	ENSP00000358994.3:p.Asn1150Thr
ENST00000369985.9:c.3380A>C	ENSP00000359002.3:p.Asn1127Thr
ENST00000664640.1:c.3476A>C	ENSP00000499278.1:p.Asn1159Thr
ENST00000671923.1:c.*1460A>C	ENSP00000500835.1:n.*1460A>C
ENST00000672093.1:c.3449A>C	ENSP00000500710.1:p.Asn1150Thr
ENST00000672162.1:n.1615A>C
ENST00000369975.5:c.3353A>C	ENSP00000358992.1:p.Asn1118Thr
ENST00000369977.7:c.3449A>C	ENSP00000358994.3:p.Asn1150Thr
ENST00000369981.7:c.3479A>C	ENSP00000358998.4:p.Asn1160Thr
ENST00000369985.8:c.3380A>C	ENSP00000359002.3:p.Asn1127Thr
ENST00000615563.4:c.3380A>C	ENSP00000478013.1:p.Asn1127Thr
ENST00000627432.2:c.3476A>C	ENSP00000487348.1:p.Asn1159Thr
NM_001300899.1:c.3380A>C	NP_001287828.1:p.Asn1127Thr
NM_004999.3:c.3449A>C	NP_004990.3:p.Asn1150Thr
XM_005248719.2:c.3476A>C	XP_005248776.1:p.Asn1159Thr
XM_005248720.2:c.3449A>C	XP_005248777.1:p.Asn1150Thr
XM_005248721.2:c.3437A>C	XP_005248778.1:p.Asn1146Thr
XM_005248722.2:c.3422A>C	XP_005248779.1:p.Asn1141Thr
XM_005248724.2:c.3410A>C	XP_005248781.1:p.Asn1137Thr
XM_005248726.2:c.3353A>C	XP_005248783.1:p.Asn1118Thr
XM_005248719.4:c.3476A>C	XP_005248776.1:p.Asn1159Thr
XM_005248720.4:c.3449A>C	XP_005248777.1:p.Asn1150Thr
XM_005248721.4:c.3437A>C	XP_005248778.1:p.Asn1146Thr
XM_005248722.4:c.3422A>C	XP_005248779.1:p.Asn1141Thr
XM_005248724.4:c.3410A>C	XP_005248781.1:p.Asn1137Thr
XM_005248726.4:c.3353A>C	XP_005248783.1:p.Asn1118Thr
XM_017010899.2:c.3383A>C	XP_016866388.1:p.Asn1128Thr
XM_024446447.1:c.3476A>C	XP_024302215.1:p.Asn1159Thr
XM_024446448.1:c.3410A>C	XP_024302216.1:p.Asn1137Thr
NM_004999.4:c.3449A>C MANE Select	NP_004990.3:p.Asn1150Thr
NM_001300899.2:c.3380A>C	NP_001287828.1:p.Asn1127Thr
NM_001368136.1:c.3353A>C	NP_001355065.1:p.Asn1118Thr
NM_001368137.1:c.3410A>C	NP_001355066.1:p.Asn1137Thr
NM_001368138.1:c.3365A>C	NP_001355067.1:p.Asn1122Thr
NM_001368865.1:c.3476A>C	NP_001355794.1:p.Asn1159Thr
NM_001368866.1:c.3449A>C	NP_001355795.1:p.Asn1150Thr
NR_160538.1:n.3678A>C