Canonical Allele Identifier: CA1984127866
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207339C= , CM000673.2:g.77207339C= GRCh38
NC_000011.9:g.76918384C= , CM000673.1:g.76918384C= GRCh37
NC_000011.8:g.76596032C= NCBI36
NG_009086.1:g.84075C=
NG_009086.2:g.84094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5793C= MANE Select ENSP00000386331.3:p.Ile1931=
ENST00000670577.1:c.3620C=
ENST00000409619.6:c.5646C= ENSP00000386635.2:p.Ile1882=
ENST00000409709.7:c.5793C= ENSP00000386331.3:p.Ile1931=
ENST00000458169.2:c.3219C= ENSP00000417017.2:p.Ile1073=
ENST00000458637.6:c.5679C= ENSP00000392185.2:p.Ile1893=
ENST00000481328.7:n.3329C=
ENST00000605744.1:n.707C=
NM_000260.3:c.5793C= NP_000251.3:p.Ile1931=
NM_001127180.1:c.5679C= NP_001120652.1:p.Ile1893=
XM_005274012.2:c.5676C= XP_005274069.1:p.Ile1892=
XM_006718558.2:c.5784C= XP_006718621.1:p.Ile1928=
XM_006718559.2:c.5679C= XP_006718622.1:p.Ile1893=
XM_006718560.2:c.5676C= XP_006718623.1:p.Ile1892=
XM_006718561.2:c.5679C= XP_006718624.1:p.Ile1893=
XM_011545044.1:c.5793C= XP_011543346.1:p.Ile1931=
XM_011545045.1:c.5787C= XP_011543347.1:p.Ile1929=
XM_011545046.1:c.5760C= XP_011543348.1:p.Ile1920=
XM_011545047.1:c.5697C= XP_011543349.1:p.Ile1899=
XM_011545048.1:c.5568C= XP_011543350.1:p.Ile1856=
XM_011545049.1:c.5556C= XP_011543351.1:p.Ile1852=
XM_011545050.1:c.5529C= XP_011543352.1:p.Ile1843=
XM_011545051.1:c.5793C= XP_011543353.1:p.Ile1931=
XR_949938.1:n.6113C=
XR_949941.1:n.6113C=
XM_011545044.2:c.5793C= XP_011543346.1:p.Ile1931=
XM_011545046.2:c.5883C= XP_011543348.2:p.Ile1961=
XM_011545050.2:c.5529C= XP_011543352.1:p.Ile1843=
XM_017017778.1:c.5877C= XP_016873267.1:p.Ile1959=
XM_017017779.1:c.5874C= XP_016873268.1:p.Ile1958=
XM_017017780.1:c.5883C= XP_016873269.1:p.Ile1961=
XM_017017781.1:c.5787C= XP_016873270.1:p.Ile1929=
XM_017017782.1:c.5769C= XP_016873271.1:p.Ile1923=
XM_017017783.1:c.5766C= XP_016873272.1:p.Ile1922=
XM_017017784.1:c.5766C= XP_016873273.1:p.Ile1922=
XM_017017785.1:c.5646C= XP_016873274.1:p.Ile1882=
XM_017017786.1:c.5883C= XP_016873275.1:p.Ile1961=
XM_017017788.1:c.5769C= XP_016873277.1:p.Ile1923=
XR_001747885.1:n.5898C=
XR_001747886.1:n.5813C=
XR_001747887.1:n.5884C=
NM_000260.4:c.5793C= MANE Select NP_000251.3:p.Ile1931=
NM_001127180.2:c.5679C= NP_001120652.1:p.Ile1893=
NM_001369365.1:c.5646C= NP_001356294.1:p.Ile1882=