Canonical Allele Identifier: CA1984131586

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214745G= , CM000673.2:g.77214745G=	GRCh38
NC_000011.9:g.76925790G= , CM000673.1:g.76925790G=	GRCh37
NC_000011.8:g.76603438G=	NCBI36
NG_009086.1:g.91481G=
NG_009086.2:g.91500G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*49G= MANE Select	ENSP00000386331.3:n.*49G=
ENST00000670577.1:c.4498G=
ENST00000409619.6:c.*49G=	ENSP00000386635.2:n.*49G=
ENST00000409709.7:c.*49G=	ENSP00000386331.3:n.*49G=
ENST00000458169.2:c.4123G=	ENSP00000417017.2:n.4123G=
ENST00000458637.6:c.*49G=	ENSP00000392185.2:n.*49G=
ENST00000481328.7:n.5247G=
ENST00000605744.1:n.2211G=
NM_000260.3:c.*49G=	NP_000251.3:n.*49G=
NM_001127180.1:c.*49G=	NP_001120652.1:n.*49G=
XM_005274012.2:c.*49G=	XP_005274069.1:n.*49G=
XM_006718561.2:c.*49G=	XP_006718624.1:n.*49G=
XR_949941.1:n.6991G=
XM_017017780.1:c.*49G=	XP_016873269.1:n.*49G=
XM_017017784.1:c.*49G=	XP_016873273.1:n.*49G=
XM_017017788.1:c.*49G=	XP_016873277.1:n.*49G=
XR_001747885.1:n.6776G=
XR_001747887.1:n.6762G=
NM_000260.4:c.*49G= MANE Select	NP_000251.3:n.*49G=
NM_001127180.2:c.*49G=	NP_001120652.1:n.*49G=
NM_001369365.1:c.*49G=	NP_001356294.1:n.*49G=