Canonical Allele Identifier: CA1984127860
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207330C= , CM000673.2:g.77207330C= GRCh38
NC_000011.9:g.76918375C= , CM000673.1:g.76918375C= GRCh37
NC_000011.8:g.76596023C= NCBI36
NG_009086.1:g.84066C=
NG_009086.2:g.84085C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5784C= MANE Select ENSP00000386331.3:p.Cys1928=
ENST00000670577.1:c.3611C=
ENST00000409619.6:c.5637C= ENSP00000386635.2:p.Cys1879=
ENST00000409709.7:c.5784C= ENSP00000386331.3:p.Cys1928=
ENST00000458169.2:c.3210C= ENSP00000417017.2:p.Cys1070=
ENST00000458637.6:c.5670C= ENSP00000392185.2:p.Cys1890=
ENST00000481328.7:n.3320C=
ENST00000605744.1:n.698C=
NM_000260.3:c.5784C= NP_000251.3:p.Cys1928=
NM_001127180.1:c.5670C= NP_001120652.1:p.Cys1890=
XM_005274012.2:c.5667C= XP_005274069.1:p.Cys1889=
XM_006718558.2:c.5775C= XP_006718621.1:p.Cys1925=
XM_006718559.2:c.5670C= XP_006718622.1:p.Cys1890=
XM_006718560.2:c.5667C= XP_006718623.1:p.Cys1889=
XM_006718561.2:c.5670C= XP_006718624.1:p.Cys1890=
XM_011545044.1:c.5784C= XP_011543346.1:p.Cys1928=
XM_011545045.1:c.5778C= XP_011543347.1:p.Cys1926=
XM_011545046.1:c.5751C= XP_011543348.1:p.Cys1917=
XM_011545047.1:c.5688C= XP_011543349.1:p.Cys1896=
XM_011545048.1:c.5559C= XP_011543350.1:p.Cys1853=
XM_011545049.1:c.5547C= XP_011543351.1:p.Cys1849=
XM_011545050.1:c.5520C= XP_011543352.1:p.Cys1840=
XM_011545051.1:c.5784C= XP_011543353.1:p.Cys1928=
XR_949938.1:n.6104C=
XR_949941.1:n.6104C=
XM_011545044.2:c.5784C= XP_011543346.1:p.Cys1928=
XM_011545046.2:c.5874C= XP_011543348.2:p.Cys1958=
XM_011545050.2:c.5520C= XP_011543352.1:p.Cys1840=
XM_017017778.1:c.5868C= XP_016873267.1:p.Cys1956=
XM_017017779.1:c.5865C= XP_016873268.1:p.Cys1955=
XM_017017780.1:c.5874C= XP_016873269.1:p.Cys1958=
XM_017017781.1:c.5778C= XP_016873270.1:p.Cys1926=
XM_017017782.1:c.5760C= XP_016873271.1:p.Cys1920=
XM_017017783.1:c.5757C= XP_016873272.1:p.Cys1919=
XM_017017784.1:c.5757C= XP_016873273.1:p.Cys1919=
XM_017017785.1:c.5637C= XP_016873274.1:p.Cys1879=
XM_017017786.1:c.5874C= XP_016873275.1:p.Cys1958=
XM_017017788.1:c.5760C= XP_016873277.1:p.Cys1920=
XR_001747885.1:n.5889C=
XR_001747886.1:n.5804C=
XR_001747887.1:n.5875C=
NM_000260.4:c.5784C= MANE Select NP_000251.3:p.Cys1928=
NM_001127180.2:c.5670C= NP_001120652.1:p.Cys1890=
NM_001369365.1:c.5637C= NP_001356294.1:p.Cys1879=