Canonical Allele Identifier: CA1984129907

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211311C= , CM000673.2:g.77211311C=	GRCh38
NC_000011.9:g.76922356C= , CM000673.1:g.76922356C=	GRCh37
NC_000011.8:g.76600004C=	NCBI36
NG_009086.1:g.88047C=
NG_009086.2:g.88066C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6211C= MANE Select	ENSP00000386331.3:p.Gln2071=
ENST00000670577.1:c.4012C=
ENST00000409619.6:c.6064C=	ENSP00000386635.2:p.Gln2022=
ENST00000409709.7:c.6211C=	ENSP00000386331.3:p.Gln2071=
ENST00000458169.2:c.3637C=	ENSP00000417017.2:p.Gln1213=
ENST00000458637.6:c.6097C=	ENSP00000392185.2:p.Gln2033=
ENST00000481328.7:n.3747C=
ENST00000526863.2:n.25+400C=
ENST00000605744.1:n.1678C=
NM_000260.3:c.6211C=	NP_000251.3:p.Gln2071=
NM_001127180.1:c.6097C=	NP_001120652.1:p.Gln2033=
XM_005274012.2:c.6094C=	XP_005274069.1:p.Gln2032=
XM_006718558.2:c.6202C=	XP_006718621.1:p.Gln2068=
XM_006718559.2:c.6097C=	XP_006718622.1:p.Gln2033=
XM_006718560.2:c.6094C=	XP_006718623.1:p.Gln2032=
XM_006718561.2:c.6097C=	XP_006718624.1:p.Gln2033=
XM_011545044.1:c.6211C=	XP_011543346.1:p.Gln2071=
XM_011545045.1:c.6205C=	XP_011543347.1:p.Gln2069=
XM_011545046.1:c.6178C=	XP_011543348.1:p.Gln2060=
XM_011545047.1:c.6115C=	XP_011543349.1:p.Gln2039=
XM_011545048.1:c.5986C=	XP_011543350.1:p.Gln1996=
XM_011545049.1:c.5974C=	XP_011543351.1:p.Gln1992=
XM_011545050.1:c.5947C=	XP_011543352.1:p.Gln1983=
XM_011545051.1:c.6211C=	XP_011543353.1:p.Gln2071=
XR_949938.1:n.6531C=
XR_949941.1:n.6505C=
XM_011545044.2:c.6211C=	XP_011543346.1:p.Gln2071=
XM_011545046.2:c.6301C=	XP_011543348.2:p.Gln2101=
XM_011545050.2:c.5947C=	XP_011543352.1:p.Gln1983=
XM_017017778.1:c.6295C=	XP_016873267.1:p.Gln2099=
XM_017017779.1:c.6292C=	XP_016873268.1:p.Gln2098=
XM_017017780.1:c.6301C=	XP_016873269.1:p.Gln2101=
XM_017017781.1:c.6205C=	XP_016873270.1:p.Gln2069=
XM_017017782.1:c.6187C=	XP_016873271.1:p.Gln2063=
XM_017017783.1:c.6184C=	XP_016873272.1:p.Gln2062=
XM_017017784.1:c.6184C=	XP_016873273.1:p.Gln2062=
XM_017017785.1:c.6064C=	XP_016873274.1:p.Gln2022=
XM_017017786.1:c.6301C=	XP_016873275.1:p.Gln2101=
XM_017017788.1:c.6187C=	XP_016873277.1:p.Gln2063=
XR_001747885.1:n.6290C=
XR_001747887.1:n.6276C=
NM_000260.4:c.6211C= MANE Select	NP_000251.3:p.Gln2071=
NM_001127180.2:c.6097C=	NP_001120652.1:p.Gln2033=
NM_001369365.1:c.6064C=	NP_001356294.1:p.Gln2022=