Canonical Allele Identifier: CA1984127232

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77206108G= , CM000673.2:g.77206108G=	GRCh38
NC_000011.9:g.76917153G= , CM000673.1:g.76917153G=	GRCh37
NC_000011.8:g.76594801G=	NCBI36
NG_009086.1:g.82844G=
NG_009086.2:g.82863G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000260.4:c.5648G= MANE Select	NP_000251.3:p.Arg1883=
ENST00000409709.9:c.5648G= MANE Select	ENSP00000386331.3:p.Arg1883=
NM_000260.3:c.5648G=	NP_000251.3:p.Arg1883=
NM_001127180.1:c.5534G=	NP_001120652.1:p.Arg1845=
NM_001127180.2:c.5534G=	NP_001120652.1:p.Arg1845=
NM_001369365.1:c.5501G=	NP_001356294.1:p.Arg1834=
ENST00000409619.6:c.5501G=	ENSP00000386635.2:p.Arg1834=
ENST00000409709.7:c.5648G=	ENSP00000386331.3:p.Arg1883=
ENST00000458169.2:c.3074G=	ENSP00000417017.2:p.Arg1025=
ENST00000458637.6:c.5534G=	ENSP00000392185.2:p.Arg1845=
ENST00000481328.7:n.3184G=
ENST00000605744.1:n.269G=
ENST00000670577.1:c.3475G=
XM_005274012.2:c.5531G=	XP_005274069.1:p.Arg1844=
XM_006718558.2:c.5639G=	XP_006718621.1:p.Arg1880=
XM_006718559.2:c.5534G=	XP_006718622.1:p.Arg1845=
XM_006718560.2:c.5531G=	XP_006718623.1:p.Arg1844=
XM_006718561.2:c.5534G=	XP_006718624.1:p.Arg1845=
XM_011545044.1:c.5648G=	XP_011543346.1:p.Arg1883=
XM_011545044.2:c.5648G=	XP_011543346.1:p.Arg1883=
XM_011545045.1:c.5642G=	XP_011543347.1:p.Arg1881=
XM_011545046.1:c.5615G=	XP_011543348.1:p.Arg1872=
XM_011545046.2:c.5738G=	XP_011543348.2:p.Arg1913=
XM_011545047.1:c.5552G=	XP_011543349.1:p.Arg1851=
XM_011545048.1:c.5423G=	XP_011543350.1:p.Arg1808=
XM_011545049.1:c.5411G=	XP_011543351.1:p.Arg1804=
XM_011545050.1:c.5384G=	XP_011543352.1:p.Arg1795=
XM_011545050.2:c.5384G=	XP_011543352.1:p.Arg1795=
XM_011545051.1:c.5648G=	XP_011543353.1:p.Arg1883=
XM_011545052.1:c.*13G=	XP_011543354.1:n.*13G=
XM_017017778.1:c.5732G=	XP_016873267.1:p.Arg1911=
XM_017017779.1:c.5729G=	XP_016873268.1:p.Arg1910=
XM_017017780.1:c.5738G=	XP_016873269.1:p.Arg1913=
XM_017017781.1:c.5642G=	XP_016873270.1:p.Arg1881=
XM_017017782.1:c.5624G=	XP_016873271.1:p.Arg1875=
XM_017017783.1:c.5621G=	XP_016873272.1:p.Arg1874=
XM_017017784.1:c.5621G=	XP_016873273.1:p.Arg1874=
XM_017017785.1:c.5501G=	XP_016873274.1:p.Arg1834=
XM_017017786.1:c.5738G=	XP_016873275.1:p.Arg1913=
XM_017017788.1:c.5624G=	XP_016873277.1:p.Arg1875=
XR_001747885.1:n.5753G=
XR_001747886.1:n.5668G=
XR_001747887.1:n.5739G=
XR_949938.1:n.5968G=
XR_949941.1:n.5968G=