Canonical Allele Identifier: CA1984129864

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211222T= , CM000673.2:g.77211222T=	GRCh38
NC_000011.9:g.76922267T= , CM000673.1:g.76922267T=	GRCh37
NC_000011.8:g.76599915T=	NCBI36
NG_009086.1:g.87958T=
NG_009086.2:g.87977T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6122T= MANE Select	ENSP00000386331.3:p.Ile2041=
ENST00000670577.1:c.3923T=
ENST00000409619.6:c.5975T=	ENSP00000386635.2:p.Ile1992=
ENST00000409709.7:c.6122T=	ENSP00000386331.3:p.Ile2041=
ENST00000458169.2:c.3548T=	ENSP00000417017.2:p.Ile1183=
ENST00000458637.6:c.6008T=	ENSP00000392185.2:p.Ile2003=
ENST00000481328.7:n.3658T=
ENST00000526863.2:n.25+311T=
ENST00000605744.1:n.1589T=
NM_000260.3:c.6122T=	NP_000251.3:p.Ile2041=
NM_001127180.1:c.6008T=	NP_001120652.1:p.Ile2003=
XM_005274012.2:c.6005T=	XP_005274069.1:p.Ile2002=
XM_006718558.2:c.6113T=	XP_006718621.1:p.Ile2038=
XM_006718559.2:c.6008T=	XP_006718622.1:p.Ile2003=
XM_006718560.2:c.6005T=	XP_006718623.1:p.Ile2002=
XM_006718561.2:c.6008T=	XP_006718624.1:p.Ile2003=
XM_011545044.1:c.6122T=	XP_011543346.1:p.Ile2041=
XM_011545045.1:c.6116T=	XP_011543347.1:p.Ile2039=
XM_011545046.1:c.6089T=	XP_011543348.1:p.Ile2030=
XM_011545047.1:c.6026T=	XP_011543349.1:p.Ile2009=
XM_011545048.1:c.5897T=	XP_011543350.1:p.Ile1966=
XM_011545049.1:c.5885T=	XP_011543351.1:p.Ile1962=
XM_011545050.1:c.5858T=	XP_011543352.1:p.Ile1953=
XM_011545051.1:c.6122T=	XP_011543353.1:p.Ile2041=
XR_949938.1:n.6442T=
XR_949941.1:n.6416T=
XM_011545044.2:c.6122T=	XP_011543346.1:p.Ile2041=
XM_011545046.2:c.6212T=	XP_011543348.2:p.Ile2071=
XM_011545050.2:c.5858T=	XP_011543352.1:p.Ile1953=
XM_017017778.1:c.6206T=	XP_016873267.1:p.Ile2069=
XM_017017779.1:c.6203T=	XP_016873268.1:p.Ile2068=
XM_017017780.1:c.6212T=	XP_016873269.1:p.Ile2071=
XM_017017781.1:c.6116T=	XP_016873270.1:p.Ile2039=
XM_017017782.1:c.6098T=	XP_016873271.1:p.Ile2033=
XM_017017783.1:c.6095T=	XP_016873272.1:p.Ile2032=
XM_017017784.1:c.6095T=	XP_016873273.1:p.Ile2032=
XM_017017785.1:c.5975T=	XP_016873274.1:p.Ile1992=
XM_017017786.1:c.6212T=	XP_016873275.1:p.Ile2071=
XM_017017788.1:c.6098T=	XP_016873277.1:p.Ile2033=
XR_001747885.1:n.6201T=
XR_001747886.1:n.6142T=
XR_001747887.1:n.6187T=
NM_000260.4:c.6122T= MANE Select	NP_000251.3:p.Ile2041=
NM_001127180.2:c.6008T=	NP_001120652.1:p.Ile2003=
NM_001369365.1:c.5975T=	NP_001356294.1:p.Ile1992=