Canonical Allele Identifier: CA1984127884
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207372A= , CM000673.2:g.77207372A= GRCh38
NC_000011.9:g.76918417A= , CM000673.1:g.76918417A= GRCh37
NC_000011.8:g.76596065A= NCBI36
NG_009086.1:g.84108A=
NG_009086.2:g.84127A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5826A= MANE Select ENSP00000386331.3:p.Gly1942=
ENST00000670577.1:c.3653A=
ENST00000409619.6:c.5679A= ENSP00000386635.2:p.Gly1893=
ENST00000409709.7:c.5826A= ENSP00000386331.3:p.Gly1942=
ENST00000458169.2:c.3252A= ENSP00000417017.2:p.Gly1084=
ENST00000458637.6:c.5712A= ENSP00000392185.2:p.Gly1904=
ENST00000481328.7:n.3362A=
ENST00000605744.1:n.740A=
NM_000260.3:c.5826A= NP_000251.3:p.Gly1942=
NM_001127180.1:c.5712A= NP_001120652.1:p.Gly1904=
XM_005274012.2:c.5709A= XP_005274069.1:p.Gly1903=
XM_006718558.2:c.5817A= XP_006718621.1:p.Gly1939=
XM_006718559.2:c.5712A= XP_006718622.1:p.Gly1904=
XM_006718560.2:c.5709A= XP_006718623.1:p.Gly1903=
XM_006718561.2:c.5712A= XP_006718624.1:p.Gly1904=
XM_011545044.1:c.5826A= XP_011543346.1:p.Gly1942=
XM_011545045.1:c.5820A= XP_011543347.1:p.Gly1940=
XM_011545046.1:c.5793A= XP_011543348.1:p.Gly1931=
XM_011545047.1:c.5730A= XP_011543349.1:p.Gly1910=
XM_011545048.1:c.5601A= XP_011543350.1:p.Gly1867=
XM_011545049.1:c.5589A= XP_011543351.1:p.Gly1863=
XM_011545050.1:c.5562A= XP_011543352.1:p.Gly1854=
XM_011545051.1:c.5826A= XP_011543353.1:p.Gly1942=
XR_949938.1:n.6146A=
XR_949941.1:n.6146A=
XM_011545044.2:c.5826A= XP_011543346.1:p.Gly1942=
XM_011545046.2:c.5916A= XP_011543348.2:p.Gly1972=
XM_011545050.2:c.5562A= XP_011543352.1:p.Gly1854=
XM_017017778.1:c.5910A= XP_016873267.1:p.Gly1970=
XM_017017779.1:c.5907A= XP_016873268.1:p.Gly1969=
XM_017017780.1:c.5916A= XP_016873269.1:p.Gly1972=
XM_017017781.1:c.5820A= XP_016873270.1:p.Gly1940=
XM_017017782.1:c.5802A= XP_016873271.1:p.Gly1934=
XM_017017783.1:c.5799A= XP_016873272.1:p.Gly1933=
XM_017017784.1:c.5799A= XP_016873273.1:p.Gly1933=
XM_017017785.1:c.5679A= XP_016873274.1:p.Gly1893=
XM_017017786.1:c.5916A= XP_016873275.1:p.Gly1972=
XM_017017788.1:c.5802A= XP_016873277.1:p.Gly1934=
XR_001747885.1:n.5931A=
XR_001747886.1:n.5846A=
XR_001747887.1:n.5917A=
NM_000260.4:c.5826A= MANE Select NP_000251.3:p.Gly1942=
NM_001127180.2:c.5712A= NP_001120652.1:p.Gly1904=
NM_001369365.1:c.5679A= NP_001356294.1:p.Gly1893=