Canonical Allele Identifier: CA1984127872
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207352C= , CM000673.2:g.77207352C= GRCh38
NC_000011.9:g.76918397C= , CM000673.1:g.76918397C= GRCh37
NC_000011.8:g.76596045C= NCBI36
NG_009086.1:g.84088C=
NG_009086.2:g.84107C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5806C= MANE Select ENSP00000386331.3:p.Leu1936=
ENST00000670577.1:c.3633C=
ENST00000409619.6:c.5659C= ENSP00000386635.2:p.Leu1887=
ENST00000409709.7:c.5806C= ENSP00000386331.3:p.Leu1936=
ENST00000458169.2:c.3232C= ENSP00000417017.2:p.Leu1078=
ENST00000458637.6:c.5692C= ENSP00000392185.2:p.Leu1898=
ENST00000481328.7:n.3342C=
ENST00000605744.1:n.720C=
NM_000260.3:c.5806C= NP_000251.3:p.Leu1936=
NM_001127180.1:c.5692C= NP_001120652.1:p.Leu1898=
XM_005274012.2:c.5689C= XP_005274069.1:p.Leu1897=
XM_006718558.2:c.5797C= XP_006718621.1:p.Leu1933=
XM_006718559.2:c.5692C= XP_006718622.1:p.Leu1898=
XM_006718560.2:c.5689C= XP_006718623.1:p.Leu1897=
XM_006718561.2:c.5692C= XP_006718624.1:p.Leu1898=
XM_011545044.1:c.5806C= XP_011543346.1:p.Leu1936=
XM_011545045.1:c.5800C= XP_011543347.1:p.Leu1934=
XM_011545046.1:c.5773C= XP_011543348.1:p.Leu1925=
XM_011545047.1:c.5710C= XP_011543349.1:p.Leu1904=
XM_011545048.1:c.5581C= XP_011543350.1:p.Leu1861=
XM_011545049.1:c.5569C= XP_011543351.1:p.Leu1857=
XM_011545050.1:c.5542C= XP_011543352.1:p.Leu1848=
XM_011545051.1:c.5806C= XP_011543353.1:p.Leu1936=
XR_949938.1:n.6126C=
XR_949941.1:n.6126C=
XM_011545044.2:c.5806C= XP_011543346.1:p.Leu1936=
XM_011545046.2:c.5896C= XP_011543348.2:p.Leu1966=
XM_011545050.2:c.5542C= XP_011543352.1:p.Leu1848=
XM_017017778.1:c.5890C= XP_016873267.1:p.Leu1964=
XM_017017779.1:c.5887C= XP_016873268.1:p.Leu1963=
XM_017017780.1:c.5896C= XP_016873269.1:p.Leu1966=
XM_017017781.1:c.5800C= XP_016873270.1:p.Leu1934=
XM_017017782.1:c.5782C= XP_016873271.1:p.Leu1928=
XM_017017783.1:c.5779C= XP_016873272.1:p.Leu1927=
XM_017017784.1:c.5779C= XP_016873273.1:p.Leu1927=
XM_017017785.1:c.5659C= XP_016873274.1:p.Leu1887=
XM_017017786.1:c.5896C= XP_016873275.1:p.Leu1966=
XM_017017788.1:c.5782C= XP_016873277.1:p.Leu1928=
XR_001747885.1:n.5911C=
XR_001747886.1:n.5826C=
XR_001747887.1:n.5897C=
NM_000260.4:c.5806C= MANE Select NP_000251.3:p.Leu1936=
NM_001127180.2:c.5692C= NP_001120652.1:p.Leu1898=
NM_001369365.1:c.5659C= NP_001356294.1:p.Leu1887=