Canonical Allele Identifier: CA1984127893
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207391A= , CM000673.2:g.77207391A= GRCh38
NC_000011.9:g.76918436A= , CM000673.1:g.76918436A= GRCh37
NC_000011.8:g.76596084A= NCBI36
NG_009086.1:g.84127A=
NG_009086.2:g.84146A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5845A= MANE Select ENSP00000386331.3:p.Ile1949=
ENST00000670577.1:c.3672A=
ENST00000409619.6:c.5698A= ENSP00000386635.2:p.Ile1900=
ENST00000409709.7:c.5845A= ENSP00000386331.3:p.Ile1949=
ENST00000458169.2:c.3271A= ENSP00000417017.2:p.Ile1091=
ENST00000458637.6:c.5731A= ENSP00000392185.2:p.Ile1911=
ENST00000481328.7:n.3381A=
ENST00000605744.1:n.759A=
NM_000260.3:c.5845A= NP_000251.3:p.Ile1949=
NM_001127180.1:c.5731A= NP_001120652.1:p.Ile1911=
XM_005274012.2:c.5728A= XP_005274069.1:p.Ile1910=
XM_006718558.2:c.5836A= XP_006718621.1:p.Ile1946=
XM_006718559.2:c.5731A= XP_006718622.1:p.Ile1911=
XM_006718560.2:c.5728A= XP_006718623.1:p.Ile1910=
XM_006718561.2:c.5731A= XP_006718624.1:p.Ile1911=
XM_011545044.1:c.5845A= XP_011543346.1:p.Ile1949=
XM_011545045.1:c.5839A= XP_011543347.1:p.Ile1947=
XM_011545046.1:c.5812A= XP_011543348.1:p.Ile1938=
XM_011545047.1:c.5749A= XP_011543349.1:p.Ile1917=
XM_011545048.1:c.5620A= XP_011543350.1:p.Ile1874=
XM_011545049.1:c.5608A= XP_011543351.1:p.Ile1870=
XM_011545050.1:c.5581A= XP_011543352.1:p.Ile1861=
XM_011545051.1:c.5845A= XP_011543353.1:p.Ile1949=
XR_949938.1:n.6165A=
XR_949941.1:n.6165A=
XM_011545044.2:c.5845A= XP_011543346.1:p.Ile1949=
XM_011545046.2:c.5935A= XP_011543348.2:p.Ile1979=
XM_011545050.2:c.5581A= XP_011543352.1:p.Ile1861=
XM_017017778.1:c.5929A= XP_016873267.1:p.Ile1977=
XM_017017779.1:c.5926A= XP_016873268.1:p.Ile1976=
XM_017017780.1:c.5935A= XP_016873269.1:p.Ile1979=
XM_017017781.1:c.5839A= XP_016873270.1:p.Ile1947=
XM_017017782.1:c.5821A= XP_016873271.1:p.Ile1941=
XM_017017783.1:c.5818A= XP_016873272.1:p.Ile1940=
XM_017017784.1:c.5818A= XP_016873273.1:p.Ile1940=
XM_017017785.1:c.5698A= XP_016873274.1:p.Ile1900=
XM_017017786.1:c.5935A= XP_016873275.1:p.Ile1979=
XM_017017788.1:c.5821A= XP_016873277.1:p.Ile1941=
XR_001747885.1:n.5950A=
XR_001747886.1:n.5865A=
XR_001747887.1:n.5936A=
NM_000260.4:c.5845A= MANE Select NP_000251.3:p.Ile1949=
NM_001127180.2:c.5731A= NP_001120652.1:p.Ile1911=
NM_001369365.1:c.5698A= NP_001356294.1:p.Ile1900=