Canonical Allele Identifier: CA1984126955

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77205599G= , CM000673.2:g.77205599G=	GRCh38
NC_000011.9:g.76916644G= , CM000673.1:g.76916644G=	GRCh37
NC_000011.8:g.76594292G=	NCBI36
NG_009086.1:g.82335G=
NG_009086.2:g.82354G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5618G= MANE Select	ENSP00000386331.3:p.Arg1873=
ENST00000670577.1:c.3445G=
ENST00000409619.6:c.5471G=	ENSP00000386635.2:p.Arg1824=
ENST00000409709.7:c.5618G=	ENSP00000386331.3:p.Arg1873=
ENST00000458169.2:c.3044G=	ENSP00000417017.2:p.Arg1015=
ENST00000458637.6:c.5504G=	ENSP00000392185.2:p.Arg1835=
ENST00000481328.7:n.3154G=
ENST00000605744.1:n.239G=
NM_000260.3:c.5618G=	NP_000251.3:p.Arg1873=
NM_001127180.1:c.5504G=	NP_001120652.1:p.Arg1835=
XM_005274012.2:c.5501G=	XP_005274069.1:p.Arg1834=
XM_006718558.2:c.5609G=	XP_006718621.1:p.Arg1870=
XM_006718559.2:c.5504G=	XP_006718622.1:p.Arg1835=
XM_006718560.2:c.5501G=	XP_006718623.1:p.Arg1834=
XM_006718561.2:c.5504G=	XP_006718624.1:p.Arg1835=
XM_011545044.1:c.5618G=	XP_011543346.1:p.Arg1873=
XM_011545045.1:c.5612G=	XP_011543347.1:p.Arg1871=
XM_011545046.1:c.5585G=	XP_011543348.1:p.Arg1862=
XM_011545047.1:c.5522G=	XP_011543349.1:p.Arg1841=
XM_011545048.1:c.5393G=	XP_011543350.1:p.Arg1798=
XM_011545049.1:c.5381G=	XP_011543351.1:p.Arg1794=
XM_011545050.1:c.5354G=	XP_011543352.1:p.Arg1785=
XM_011545051.1:c.5618G=	XP_011543353.1:p.Arg1873=
XM_011545052.1:c.5533G=	XP_011543354.1:p.Gly1845=
XR_949938.1:n.5938G=
XR_949941.1:n.5938G=
XR_949942.1:n.5841G=
XM_011545044.2:c.5618G=	XP_011543346.1:p.Arg1873=
XM_011545046.2:c.5708G=	XP_011543348.2:p.Arg1903=
XM_011545050.2:c.5354G=	XP_011543352.1:p.Arg1785=
XM_017017778.1:c.5702G=	XP_016873267.1:p.Arg1901=
XM_017017779.1:c.5699G=	XP_016873268.1:p.Arg1900=
XM_017017780.1:c.5708G=	XP_016873269.1:p.Arg1903=
XM_017017781.1:c.5612G=	XP_016873270.1:p.Arg1871=
XM_017017782.1:c.5594G=	XP_016873271.1:p.Arg1865=
XM_017017783.1:c.5591G=	XP_016873272.1:p.Arg1864=
XM_017017784.1:c.5591G=	XP_016873273.1:p.Arg1864=
XM_017017785.1:c.5471G=	XP_016873274.1:p.Arg1824=
XM_017017786.1:c.5708G=	XP_016873275.1:p.Arg1903=
XM_017017788.1:c.5594G=	XP_016873277.1:p.Arg1865=
XR_001747885.1:n.5723G=
XR_001747886.1:n.5638G=
XR_001747887.1:n.5709G=
XR_001747888.1:n.5624G=
NM_000260.4:c.5618G= MANE Select	NP_000251.3:p.Arg1873=
NM_001127180.2:c.5504G=	NP_001120652.1:p.Arg1835=
NM_001369365.1:c.5471G=	NP_001356294.1:p.Arg1824=