Canonical Allele Identifier: CA1984113467

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77182101C= , CM000673.2:g.77182101C=	GRCh38
NC_000011.8:g.76570795C=	NCBI36
NG_009086.1:g.58838C=
NG_009086.2:g.58856C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.3055C= MANE Select	ENSP00000386331.3:p.Arg1019=
ENST00000409893.6:c.1120C=	ENSP00000386689.2:p.Arg374=
ENST00000670577.1:c.896C=
ENST00000409619.6:c.3022C=	ENSP00000386635.2:p.Arg1008=
ENST00000409709.7:c.3055C=	ENSP00000386331.3:p.Arg1019=
ENST00000409893.5:c.3055C=	ENSP00000386689.1:p.Arg1019=
ENST00000458169.2:c.598C=	ENSP00000417017.2:p.Arg200=
ENST00000458637.6:c.3055C=	ENSP00000392185.2:p.Arg1019=
ENST00000481328.7:n.598C=
ENST00000620575.4:c.3055C=	ENSP00000477640.1:p.Arg1019=
NM_000260.3:c.3055C=	NP_000251.3:p.Arg1019=
NM_001127179.2:c.3055C=	NP_001120651.2:p.Arg1019=
NM_001127180.1:c.3055C=	NP_001120652.1:p.Arg1019=
XM_005274012.2:c.3055C=	XP_005274069.1:p.Arg1019=
XM_006718558.2:c.3055C=	XP_006718621.1:p.Arg1019=
XM_006718559.2:c.3055C=	XP_006718622.1:p.Arg1019=
XM_006718560.2:c.3055C=	XP_006718623.1:p.Arg1019=
XM_006718561.2:c.3055C=	XP_006718624.1:p.Arg1019=
XM_011545044.1:c.3055C=	XP_011543346.1:p.Arg1019=
XM_011545045.1:c.3055C=	XP_011543347.1:p.Arg1019=
XM_011545046.1:c.3022C=	XP_011543348.1:p.Arg1008=
XM_011545047.1:c.3055C=	XP_011543349.1:p.Arg1019=
XM_011545048.1:c.2836C=	XP_011543350.1:p.Arg946=
XM_011545049.1:c.2824C=	XP_011543351.1:p.Arg942=
XM_011545050.1:c.2797C=	XP_011543352.1:p.Arg933=
XM_011545051.1:c.3055C=	XP_011543353.1:p.Arg1019=
XM_011545052.1:c.3055C=	XP_011543354.1:p.Arg1019=
XR_949938.1:n.3375C=
XR_949941.1:n.3375C=
XR_949942.1:n.3377C=
XR_949943.1:n.3377C=
XM_011545044.2:c.3055C=	XP_011543346.1:p.Arg1019=
XM_011545046.2:c.3145C=	XP_011543348.2:p.Arg1049=
XM_011545050.2:c.2797C=	XP_011543352.1:p.Arg933=
XM_017017778.1:c.3145C=	XP_016873267.1:p.Arg1049=
XM_017017779.1:c.3145C=	XP_016873268.1:p.Arg1049=
XM_017017780.1:c.3145C=	XP_016873269.1:p.Arg1049=
XM_017017781.1:c.3145C=	XP_016873270.1:p.Arg1049=
XM_017017782.1:c.3145C=	XP_016873271.1:p.Arg1049=
XM_017017783.1:c.3145C=	XP_016873272.1:p.Arg1049=
XM_017017784.1:c.3145C=	XP_016873273.1:p.Arg1049=
XM_017017785.1:c.2914C=	XP_016873274.1:p.Arg972=
XM_017017786.1:c.3145C=	XP_016873275.1:p.Arg1049=
XM_017017787.1:c.3145C=	XP_016873276.1:p.Arg1049=
XM_017017788.1:c.3145C=	XP_016873277.1:p.Arg1049=
XR_001747885.1:n.3160C=
XR_001747886.1:n.3160C=
XR_001747887.1:n.3160C=
XR_001747888.1:n.3160C=
XR_001747889.1:n.3160C=
NM_000260.4:c.3055C= MANE Select	NP_000251.3:p.Arg1019=
NM_001127180.2:c.3055C=	NP_001120652.1:p.Arg1019=
NM_001369365.1:c.3022C=	NP_001356294.1:p.Arg1008=