Canonical Allele Identifier: CA1984127877
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207361T= , CM000673.2:g.77207361T= GRCh38
NC_000011.9:g.76918406T= , CM000673.1:g.76918406T= GRCh37
NC_000011.8:g.76596054T= NCBI36
NG_009086.1:g.84097T=
NG_009086.2:g.84116T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5815T= MANE Select ENSP00000386331.3:p.Ser1939=
ENST00000670577.1:c.3642T=
ENST00000409619.6:c.5668T= ENSP00000386635.2:p.Ser1890=
ENST00000409709.7:c.5815T= ENSP00000386331.3:p.Ser1939=
ENST00000458169.2:c.3241T= ENSP00000417017.2:p.Ser1081=
ENST00000458637.6:c.5701T= ENSP00000392185.2:p.Ser1901=
ENST00000481328.7:n.3351T=
ENST00000605744.1:n.729T=
NM_000260.3:c.5815T= NP_000251.3:p.Ser1939=
NM_001127180.1:c.5701T= NP_001120652.1:p.Ser1901=
XM_005274012.2:c.5698T= XP_005274069.1:p.Ser1900=
XM_006718558.2:c.5806T= XP_006718621.1:p.Ser1936=
XM_006718559.2:c.5701T= XP_006718622.1:p.Ser1901=
XM_006718560.2:c.5698T= XP_006718623.1:p.Ser1900=
XM_006718561.2:c.5701T= XP_006718624.1:p.Ser1901=
XM_011545044.1:c.5815T= XP_011543346.1:p.Ser1939=
XM_011545045.1:c.5809T= XP_011543347.1:p.Ser1937=
XM_011545046.1:c.5782T= XP_011543348.1:p.Ser1928=
XM_011545047.1:c.5719T= XP_011543349.1:p.Ser1907=
XM_011545048.1:c.5590T= XP_011543350.1:p.Ser1864=
XM_011545049.1:c.5578T= XP_011543351.1:p.Ser1860=
XM_011545050.1:c.5551T= XP_011543352.1:p.Ser1851=
XM_011545051.1:c.5815T= XP_011543353.1:p.Ser1939=
XR_949938.1:n.6135T=
XR_949941.1:n.6135T=
XM_011545044.2:c.5815T= XP_011543346.1:p.Ser1939=
XM_011545046.2:c.5905T= XP_011543348.2:p.Ser1969=
XM_011545050.2:c.5551T= XP_011543352.1:p.Ser1851=
XM_017017778.1:c.5899T= XP_016873267.1:p.Ser1967=
XM_017017779.1:c.5896T= XP_016873268.1:p.Ser1966=
XM_017017780.1:c.5905T= XP_016873269.1:p.Ser1969=
XM_017017781.1:c.5809T= XP_016873270.1:p.Ser1937=
XM_017017782.1:c.5791T= XP_016873271.1:p.Ser1931=
XM_017017783.1:c.5788T= XP_016873272.1:p.Ser1930=
XM_017017784.1:c.5788T= XP_016873273.1:p.Ser1930=
XM_017017785.1:c.5668T= XP_016873274.1:p.Ser1890=
XM_017017786.1:c.5905T= XP_016873275.1:p.Ser1969=
XM_017017788.1:c.5791T= XP_016873277.1:p.Ser1931=
XR_001747885.1:n.5920T=
XR_001747886.1:n.5835T=
XR_001747887.1:n.5906T=
NM_000260.4:c.5815T= MANE Select NP_000251.3:p.Ser1939=
NM_001127180.2:c.5701T= NP_001120652.1:p.Ser1901=
NM_001369365.1:c.5668T= NP_001356294.1:p.Ser1890=