Canonical Allele Identifier: CA1984129914

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211329_77211330delinsTG , CM000673.2:g.77211329_77211330delinsTG	GRCh38
NC_000011.9:g.76922374_76922375delinsTG , CM000673.1:g.76922374_76922375delinsTG	GRCh37
NC_000011.8:g.76600022_76600023delinsTG	NCBI36
NG_009086.1:g.88065_88066delinsTG
NG_009086.2:g.88084_88085delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6229_6230delinsTG MANE Select	ENSP00000386331.3:p.Trp2077=
ENST00000670577.1:c.4030_4031delinsTG
ENST00000409619.6:c.6082_6083delinsTG	ENSP00000386635.2:p.Trp2028=
ENST00000409709.7:c.6229_6230delinsTG	ENSP00000386331.3:p.Trp2077=
ENST00000458169.2:c.3655_3656delinsTG	ENSP00000417017.2:p.Trp1219=
ENST00000458637.6:c.6115_6116delinsTG	ENSP00000392185.2:p.Trp2039=
ENST00000481328.7:n.3765_3766delinsTG
ENST00000526863.2:n.25+418_25+419delinsTG
ENST00000605744.1:n.1696_1697delinsTG
NM_000260.3:c.6229_6230delinsTG	NP_000251.3:p.Trp2077=
NM_001127180.1:c.6115_6116delinsTG	NP_001120652.1:p.Trp2039=
XM_005274012.2:c.6112_6113delinsTG	XP_005274069.1:p.Trp2038=
XM_006718558.2:c.6220_6221delinsTG	XP_006718621.1:p.Trp2074=
XM_006718559.2:c.6115_6116delinsTG	XP_006718622.1:p.Trp2039=
XM_006718560.2:c.6112_6113delinsTG	XP_006718623.1:p.Trp2038=
XM_006718561.2:c.6115_6116delinsTG	XP_006718624.1:p.Trp2039=
XM_011545044.1:c.6229_6230delinsTG	XP_011543346.1:p.Trp2077=
XM_011545045.1:c.6223_6224delinsTG	XP_011543347.1:p.Trp2075=
XM_011545046.1:c.6196_6197delinsTG	XP_011543348.1:p.Trp2066=
XM_011545047.1:c.6133_6134delinsTG	XP_011543349.1:p.Trp2045=
XM_011545048.1:c.6004_6005delinsTG	XP_011543350.1:p.Trp2002=
XM_011545049.1:c.5992_5993delinsTG	XP_011543351.1:p.Trp1998=
XM_011545050.1:c.5965_5966delinsTG	XP_011543352.1:p.Trp1989=
XM_011545051.1:c.6229_6230delinsTG	XP_011543353.1:p.Trp2077=
XR_949938.1:n.6549_6550delinsTG
XR_949941.1:n.6523_6524delinsTG
XM_011545044.2:c.6229_6230delinsTG	XP_011543346.1:p.Trp2077=
XM_011545046.2:c.6319_6320delinsTG	XP_011543348.2:p.Trp2107=
XM_011545050.2:c.5965_5966delinsTG	XP_011543352.1:p.Trp1989=
XM_017017778.1:c.6313_6314delinsTG	XP_016873267.1:p.Trp2105=
XM_017017779.1:c.6310_6311delinsTG	XP_016873268.1:p.Trp2104=
XM_017017780.1:c.6319_6320delinsTG	XP_016873269.1:p.Trp2107=
XM_017017781.1:c.6223_6224delinsTG	XP_016873270.1:p.Trp2075=
XM_017017782.1:c.6205_6206delinsTG	XP_016873271.1:p.Trp2069=
XM_017017783.1:c.6202_6203delinsTG	XP_016873272.1:p.Trp2068=
XM_017017784.1:c.6202_6203delinsTG	XP_016873273.1:p.Trp2068=
XM_017017785.1:c.6082_6083delinsTG	XP_016873274.1:p.Trp2028=
XM_017017786.1:c.6319_6320delinsTG	XP_016873275.1:p.Trp2107=
XM_017017788.1:c.6205_6206delinsTG	XP_016873277.1:p.Trp2069=
XR_001747885.1:n.6308_6309delinsTG
XR_001747887.1:n.6294_6295delinsTG
NM_000260.4:c.6229_6230delinsTG MANE Select	NP_000251.3:p.Trp2077=
NM_001127180.2:c.6115_6116delinsTG	NP_001120652.1:p.Trp2039=
NM_001369365.1:c.6082_6083delinsTG	NP_001356294.1:p.Trp2028=