Canonical Allele Identifier: CA1984131558

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214694T= , CM000673.2:g.77214694T=	GRCh38
NC_000011.9:g.76925739T= , CM000673.1:g.76925739T=	GRCh37
NC_000011.8:g.76603387T=	NCBI36
NG_009086.1:g.91430T=
NG_009086.2:g.91449T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6646T= MANE Select	ENSP00000386331.3:p.Ter2216=
ENST00000670577.1:c.4447T=
ENST00000409619.6:c.6499T=	ENSP00000386635.2:p.Ter2167=
ENST00000409709.7:c.6646T=	ENSP00000386331.3:p.Ter2216=
ENST00000458169.2:c.4072T=	ENSP00000417017.2:p.Ter1358=
ENST00000458637.6:c.6526T=	ENSP00000392185.2:p.Ter2176=
ENST00000481328.7:n.5196T=
ENST00000605744.1:n.2160T=
NM_000260.3:c.6646T=	NP_000251.3:p.Ter2216=
NM_001127180.1:c.6526T=	NP_001120652.1:p.Ter2176=
XM_005274012.2:c.6529T=	XP_005274069.1:p.Ter2177=
XM_006718561.2:c.6532T=	XP_006718624.1:p.Ter2178=
XR_949941.1:n.6940T=
XM_017017780.1:c.6736T=	XP_016873269.1:p.Ter2246=
XM_017017784.1:c.6619T=	XP_016873273.1:p.Ter2207=
XM_017017788.1:c.6622T=	XP_016873277.1:p.Ter2208=
XR_001747885.1:n.6725T=
XR_001747887.1:n.6711T=
NM_000260.4:c.6646T= MANE Select	NP_000251.3:p.Ter2216=
NM_001127180.2:c.6526T=	NP_001120652.1:p.Ter2176=
NM_001369365.1:c.6499T=	NP_001356294.1:p.Ter2167=