Canonical Allele Identifier: CA1984128575
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77208720C= , CM000673.2:g.77208720C= GRCh38
NC_000011.9:g.76919765C= , CM000673.1:g.76919765C= GRCh37
NC_000011.8:g.76597413C= NCBI36
NG_009086.1:g.85456C=
NG_009086.2:g.85475C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5968C= MANE Select ENSP00000386331.3:p.Gln1990=
ENST00000670577.1:c.3772-3C=
ENST00000409619.6:c.5821C= ENSP00000386635.2:p.Gln1941=
ENST00000409709.7:c.5968C= ENSP00000386331.3:p.Gln1990=
ENST00000458169.2:c.3394C= ENSP00000417017.2:p.Gln1132=
ENST00000458637.6:c.5854C= ENSP00000392185.2:p.Gln1952=
ENST00000481328.7:n.3504C=
ENST00000605744.1:n.882C=
NM_000260.3:c.5968C= NP_000251.3:p.Gln1990=
NM_001127180.1:c.5854C= NP_001120652.1:p.Gln1952=
XM_005274012.2:c.5851C= XP_005274069.1:p.Gln1951=
XM_006718558.2:c.5959C= XP_006718621.1:p.Gln1987=
XM_006718559.2:c.5854C= XP_006718622.1:p.Gln1952=
XM_006718560.2:c.5851C= XP_006718623.1:p.Gln1951=
XM_006718561.2:c.5854C= XP_006718624.1:p.Gln1952=
XM_011545044.1:c.5968C= XP_011543346.1:p.Gln1990=
XM_011545045.1:c.5962C= XP_011543347.1:p.Gln1988=
XM_011545046.1:c.5935C= XP_011543348.1:p.Gln1979=
XM_011545047.1:c.5872C= XP_011543349.1:p.Gln1958=
XM_011545048.1:c.5743C= XP_011543350.1:p.Gln1915=
XM_011545049.1:c.5731C= XP_011543351.1:p.Gln1911=
XM_011545050.1:c.5704C= XP_011543352.1:p.Gln1902=
XM_011545051.1:c.5968C= XP_011543353.1:p.Gln1990=
XR_949938.1:n.6288C=
XR_949941.1:n.6265-3C=
XM_011545044.2:c.5968C= XP_011543346.1:p.Gln1990=
XM_011545046.2:c.6058C= XP_011543348.2:p.Gln2020=
XM_011545050.2:c.5704C= XP_011543352.1:p.Gln1902=
XM_017017778.1:c.6052C= XP_016873267.1:p.Gln2018=
XM_017017779.1:c.6049C= XP_016873268.1:p.Gln2017=
XM_017017780.1:c.6058C= XP_016873269.1:p.Gln2020=
XM_017017781.1:c.5962C= XP_016873270.1:p.Gln1988=
XM_017017782.1:c.5944C= XP_016873271.1:p.Gln1982=
XM_017017783.1:c.5941C= XP_016873272.1:p.Gln1981=
XM_017017784.1:c.5941C= XP_016873273.1:p.Gln1981=
XM_017017785.1:c.5821C= XP_016873274.1:p.Gln1941=
XM_017017786.1:c.6058C= XP_016873275.1:p.Gln2020=
XM_017017788.1:c.5944C= XP_016873277.1:p.Gln1982=
XR_001747885.1:n.6050-3C=
XR_001747886.1:n.5988C=
XR_001747887.1:n.6036-3C=
NM_000260.4:c.5968C= MANE Select NP_000251.3:p.Gln1990=
NM_001127180.2:c.5854C= NP_001120652.1:p.Gln1952=
NM_001369365.1:c.5821C= NP_001356294.1:p.Gln1941=