Canonical Allele Identifier: CA1984125260

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77202357C= , CM000673.2:g.77202357C=	GRCh38
NC_000011.9:g.76913402C= , CM000673.1:g.76913402C=	GRCh37
NC_000011.8:g.76591050C=	NCBI36
NG_009086.1:g.79093C=
NG_009086.2:g.79112C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000260.4:c.5101C= MANE Select	NP_000251.3:p.Arg1701=
ENST00000409709.9:c.5101C= MANE Select	ENSP00000386331.3:p.Arg1701=
NM_000260.3:c.5101C=	NP_000251.3:p.Arg1701=
NM_001127180.1:c.4987C=	NP_001120652.1:p.Arg1663=
NM_001127180.2:c.4987C=	NP_001120652.1:p.Arg1663=
NM_001369365.1:c.4954C=	NP_001356294.1:p.Arg1652=
ENST00000409619.6:c.4954C=	ENSP00000386635.2:p.Arg1652=
ENST00000409709.7:c.5101C=	ENSP00000386331.3:p.Arg1701=
ENST00000458169.2:c.2527C=	ENSP00000417017.2:p.Arg843=
ENST00000458637.6:c.4987C=	ENSP00000392185.2:p.Arg1663=
ENST00000481328.7:n.2637C=
ENST00000670577.1:c.2942C=
XM_005274012.2:c.4984C=	XP_005274069.1:p.Arg1662=
XM_006718558.2:c.5092C=	XP_006718621.1:p.Arg1698=
XM_006718559.2:c.4987C=	XP_006718622.1:p.Arg1663=
XM_006718560.2:c.4984C=	XP_006718623.1:p.Arg1662=
XM_006718561.2:c.4987C=	XP_006718624.1:p.Arg1663=
XM_011545044.1:c.5101C=	XP_011543346.1:p.Arg1701=
XM_011545044.2:c.5101C=	XP_011543346.1:p.Arg1701=
XM_011545045.1:c.5095C=	XP_011543347.1:p.Arg1699=
XM_011545046.1:c.5068C=	XP_011543348.1:p.Arg1690=
XM_011545046.2:c.5191C=	XP_011543348.2:p.Arg1731=
XM_011545047.1:c.5005C=	XP_011543349.1:p.Arg1669=
XM_011545048.1:c.4876C=	XP_011543350.1:p.Arg1626=
XM_011545049.1:c.4864C=	XP_011543351.1:p.Arg1622=
XM_011545050.1:c.4837C=	XP_011543352.1:p.Arg1613=
XM_011545050.2:c.4837C=	XP_011543352.1:p.Arg1613=
XM_011545051.1:c.5101C=	XP_011543353.1:p.Arg1701=
XM_011545052.1:c.5101C=	XP_011543354.1:p.Arg1701=
XM_017017778.1:c.5185C=	XP_016873267.1:p.Arg1729=
XM_017017779.1:c.5182C=	XP_016873268.1:p.Arg1728=
XM_017017780.1:c.5191C=	XP_016873269.1:p.Arg1731=
XM_017017781.1:c.5095C=	XP_016873270.1:p.Arg1699=
XM_017017782.1:c.5077C=	XP_016873271.1:p.Arg1693=
XM_017017783.1:c.5074C=	XP_016873272.1:p.Arg1692=
XM_017017784.1:c.5074C=	XP_016873273.1:p.Arg1692=
XM_017017785.1:c.4954C=	XP_016873274.1:p.Arg1652=
XM_017017786.1:c.5191C=	XP_016873275.1:p.Arg1731=
XM_017017788.1:c.5077C=	XP_016873277.1:p.Arg1693=
XR_001747885.1:n.5206C=
XR_001747886.1:n.5206C=
XR_001747887.1:n.5206C=
XR_001747888.1:n.5206C=
XR_949938.1:n.5421C=
XR_949941.1:n.5421C=
XR_949942.1:n.5423C=