Canonical Allele Identifier: CA475792825

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76925720G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214675G>A , CM000673.2:g.77214675G>A	GRCh38
NC_000011.9:g.76925720G>A , CM000673.1:g.76925720G>A	GRCh37
NC_000011.8:g.76603368G>A	NCBI36
NG_009086.1:g.91411G>A
NG_009086.2:g.91430G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6627G>A MANE Select	ENSP00000386331.3:p.Arg2209=
ENST00000670577.1:c.4428G>A
ENST00000409619.6:c.6480G>A	ENSP00000386635.2:p.Arg2160=
ENST00000409709.7:c.6627G>A	ENSP00000386331.3:p.Arg2209=
ENST00000458169.2:c.4053G>A	ENSP00000417017.2:p.Arg1351=
ENST00000458637.6:c.6507G>A	ENSP00000392185.2:p.Arg2169=
ENST00000481328.7:n.5177G>A
ENST00000605744.1:n.2141G>A
NM_000260.3:c.6627G>A	NP_000251.3:p.Arg2209=
NM_001127180.1:c.6507G>A	NP_001120652.1:p.Arg2169=
XM_005274012.2:c.6510G>A	XP_005274069.1:p.Arg2170=
XM_006718561.2:c.6513G>A	XP_006718624.1:p.Arg2171=
XR_949941.1:n.6921G>A
XM_017017780.1:c.6717G>A	XP_016873269.1:p.Arg2239=
XM_017017784.1:c.6600G>A	XP_016873273.1:p.Arg2200=
XM_017017788.1:c.6603G>A	XP_016873277.1:p.Arg2201=
XR_001747885.1:n.6706G>A
XR_001747887.1:n.6692G>A
NM_000260.4:c.6627G>A MANE Select	NP_000251.3:p.Arg2209=
NM_001127180.2:c.6507G>A	NP_001120652.1:p.Arg2169=
NM_001369365.1:c.6480G>A	NP_001356294.1:p.Arg2160=