Canonical Allele Identifier: CA1984129867

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211227A= , CM000673.2:g.77211227A=	GRCh38
NC_000011.9:g.76922272A= , CM000673.1:g.76922272A=	GRCh37
NC_000011.8:g.76599920A=	NCBI36
NG_009086.1:g.87963A=
NG_009086.2:g.87982A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6127A= MANE Select	ENSP00000386331.3:p.Arg2043=
ENST00000670577.1:c.3928A=
ENST00000409619.6:c.5980A=	ENSP00000386635.2:p.Arg1994=
ENST00000409709.7:c.6127A=	ENSP00000386331.3:p.Arg2043=
ENST00000458169.2:c.3553A=	ENSP00000417017.2:p.Arg1185=
ENST00000458637.6:c.6013A=	ENSP00000392185.2:p.Arg2005=
ENST00000481328.7:n.3663A=
ENST00000526863.2:n.25+316A=
ENST00000605744.1:n.1594A=
NM_000260.3:c.6127A=	NP_000251.3:p.Arg2043=
NM_001127180.1:c.6013A=	NP_001120652.1:p.Arg2005=
XM_005274012.2:c.6010A=	XP_005274069.1:p.Arg2004=
XM_006718558.2:c.6118A=	XP_006718621.1:p.Arg2040=
XM_006718559.2:c.6013A=	XP_006718622.1:p.Arg2005=
XM_006718560.2:c.6010A=	XP_006718623.1:p.Arg2004=
XM_006718561.2:c.6013A=	XP_006718624.1:p.Arg2005=
XM_011545044.1:c.6127A=	XP_011543346.1:p.Arg2043=
XM_011545045.1:c.6121A=	XP_011543347.1:p.Arg2041=
XM_011545046.1:c.6094A=	XP_011543348.1:p.Arg2032=
XM_011545047.1:c.6031A=	XP_011543349.1:p.Arg2011=
XM_011545048.1:c.5902A=	XP_011543350.1:p.Arg1968=
XM_011545049.1:c.5890A=	XP_011543351.1:p.Arg1964=
XM_011545050.1:c.5863A=	XP_011543352.1:p.Arg1955=
XM_011545051.1:c.6127A=	XP_011543353.1:p.Arg2043=
XR_949938.1:n.6447A=
XR_949941.1:n.6421A=
XM_011545044.2:c.6127A=	XP_011543346.1:p.Arg2043=
XM_011545046.2:c.6217A=	XP_011543348.2:p.Arg2073=
XM_011545050.2:c.5863A=	XP_011543352.1:p.Arg1955=
XM_017017778.1:c.6211A=	XP_016873267.1:p.Arg2071=
XM_017017779.1:c.6208A=	XP_016873268.1:p.Arg2070=
XM_017017780.1:c.6217A=	XP_016873269.1:p.Arg2073=
XM_017017781.1:c.6121A=	XP_016873270.1:p.Arg2041=
XM_017017782.1:c.6103A=	XP_016873271.1:p.Arg2035=
XM_017017783.1:c.6100A=	XP_016873272.1:p.Arg2034=
XM_017017784.1:c.6100A=	XP_016873273.1:p.Arg2034=
XM_017017785.1:c.5980A=	XP_016873274.1:p.Arg1994=
XM_017017786.1:c.6217A=	XP_016873275.1:p.Arg2073=
XM_017017788.1:c.6103A=	XP_016873277.1:p.Arg2035=
XR_001747885.1:n.6206A=
XR_001747886.1:n.6147A=
XR_001747887.1:n.6192A=
NM_000260.4:c.6127A= MANE Select	NP_000251.3:p.Arg2043=
NM_001127180.2:c.6013A=	NP_001120652.1:p.Arg2005=
NM_001369365.1:c.5980A=	NP_001356294.1:p.Arg1994=