Canonical Allele Identifier: CA1984127857
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207324C= , CM000673.2:g.77207324C= GRCh38
NC_000011.9:g.76918369C= , CM000673.1:g.76918369C= GRCh37
NC_000011.8:g.76596017C= NCBI36
NG_009086.1:g.84060C=
NG_009086.2:g.84079C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5778C= MANE Select ENSP00000386331.3:p.Asp1926=
ENST00000670577.1:c.3605C=
ENST00000409619.6:c.5631C= ENSP00000386635.2:p.Asp1877=
ENST00000409709.7:c.5778C= ENSP00000386331.3:p.Asp1926=
ENST00000458169.2:c.3204C= ENSP00000417017.2:p.Asp1068=
ENST00000458637.6:c.5664C= ENSP00000392185.2:p.Asp1888=
ENST00000481328.7:n.3314C=
ENST00000605744.1:n.692C=
NM_000260.3:c.5778C= NP_000251.3:p.Asp1926=
NM_001127180.1:c.5664C= NP_001120652.1:p.Asp1888=
XM_005274012.2:c.5661C= XP_005274069.1:p.Asp1887=
XM_006718558.2:c.5769C= XP_006718621.1:p.Asp1923=
XM_006718559.2:c.5664C= XP_006718622.1:p.Asp1888=
XM_006718560.2:c.5661C= XP_006718623.1:p.Asp1887=
XM_006718561.2:c.5664C= XP_006718624.1:p.Asp1888=
XM_011545044.1:c.5778C= XP_011543346.1:p.Asp1926=
XM_011545045.1:c.5772C= XP_011543347.1:p.Asp1924=
XM_011545046.1:c.5745C= XP_011543348.1:p.Asp1915=
XM_011545047.1:c.5682C= XP_011543349.1:p.Asp1894=
XM_011545048.1:c.5553C= XP_011543350.1:p.Asp1851=
XM_011545049.1:c.5541C= XP_011543351.1:p.Asp1847=
XM_011545050.1:c.5514C= XP_011543352.1:p.Asp1838=
XM_011545051.1:c.5778C= XP_011543353.1:p.Asp1926=
XR_949938.1:n.6098C=
XR_949941.1:n.6098C=
XM_011545044.2:c.5778C= XP_011543346.1:p.Asp1926=
XM_011545046.2:c.5868C= XP_011543348.2:p.Asp1956=
XM_011545050.2:c.5514C= XP_011543352.1:p.Asp1838=
XM_017017778.1:c.5862C= XP_016873267.1:p.Asp1954=
XM_017017779.1:c.5859C= XP_016873268.1:p.Asp1953=
XM_017017780.1:c.5868C= XP_016873269.1:p.Asp1956=
XM_017017781.1:c.5772C= XP_016873270.1:p.Asp1924=
XM_017017782.1:c.5754C= XP_016873271.1:p.Asp1918=
XM_017017783.1:c.5751C= XP_016873272.1:p.Asp1917=
XM_017017784.1:c.5751C= XP_016873273.1:p.Asp1917=
XM_017017785.1:c.5631C= XP_016873274.1:p.Asp1877=
XM_017017786.1:c.5868C= XP_016873275.1:p.Asp1956=
XM_017017788.1:c.5754C= XP_016873277.1:p.Asp1918=
XR_001747885.1:n.5883C=
XR_001747886.1:n.5798C=
XR_001747887.1:n.5869C=
NM_000260.4:c.5778C= MANE Select NP_000251.3:p.Asp1926=
NM_001127180.2:c.5664C= NP_001120652.1:p.Asp1888=
NM_001369365.1:c.5631C= NP_001356294.1:p.Asp1877=