Canonical Allele Identifier: CA1984129845
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77211193G= , CM000673.2:g.77211193G= GRCh38
NC_000011.9:g.76922238G= , CM000673.1:g.76922238G= GRCh37
NC_000011.8:g.76599886G= NCBI36
NG_009086.1:g.87929G=
NG_009086.2:g.87948G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.6093G= MANE Select ENSP00000386331.3:p.Arg2031=
ENST00000670577.1:c.3894G=
ENST00000409619.6:c.5946G= ENSP00000386635.2:p.Arg1982=
ENST00000409709.7:c.6093G= ENSP00000386331.3:p.Arg2031=
ENST00000458169.2:c.3519G= ENSP00000417017.2:p.Arg1173=
ENST00000458637.6:c.5979G= ENSP00000392185.2:p.Arg1993=
ENST00000481328.7:n.3629G=
ENST00000526863.2:n.25+282G=
ENST00000605744.1:n.1560G=
NM_000260.3:c.6093G= NP_000251.3:p.Arg2031=
NM_001127180.1:c.5979G= NP_001120652.1:p.Arg1993=
XM_005274012.2:c.5976G= XP_005274069.1:p.Arg1992=
XM_006718558.2:c.6084G= XP_006718621.1:p.Arg2028=
XM_006718559.2:c.5979G= XP_006718622.1:p.Arg1993=
XM_006718560.2:c.5976G= XP_006718623.1:p.Arg1992=
XM_006718561.2:c.5979G= XP_006718624.1:p.Arg1993=
XM_011545044.1:c.6093G= XP_011543346.1:p.Arg2031=
XM_011545045.1:c.6087G= XP_011543347.1:p.Arg2029=
XM_011545046.1:c.6060G= XP_011543348.1:p.Arg2020=
XM_011545047.1:c.5997G= XP_011543349.1:p.Arg1999=
XM_011545048.1:c.5868G= XP_011543350.1:p.Arg1956=
XM_011545049.1:c.5856G= XP_011543351.1:p.Arg1952=
XM_011545050.1:c.5829G= XP_011543352.1:p.Arg1943=
XM_011545051.1:c.6093G= XP_011543353.1:p.Arg2031=
XR_949938.1:n.6413G=
XR_949941.1:n.6387G=
XM_011545044.2:c.6093G= XP_011543346.1:p.Arg2031=
XM_011545046.2:c.6183G= XP_011543348.2:p.Arg2061=
XM_011545050.2:c.5829G= XP_011543352.1:p.Arg1943=
XM_017017778.1:c.6177G= XP_016873267.1:p.Arg2059=
XM_017017779.1:c.6174G= XP_016873268.1:p.Arg2058=
XM_017017780.1:c.6183G= XP_016873269.1:p.Arg2061=
XM_017017781.1:c.6087G= XP_016873270.1:p.Arg2029=
XM_017017782.1:c.6069G= XP_016873271.1:p.Arg2023=
XM_017017783.1:c.6066G= XP_016873272.1:p.Arg2022=
XM_017017784.1:c.6066G= XP_016873273.1:p.Arg2022=
XM_017017785.1:c.5946G= XP_016873274.1:p.Arg1982=
XM_017017786.1:c.6183G= XP_016873275.1:p.Arg2061=
XM_017017788.1:c.6069G= XP_016873277.1:p.Arg2023=
XR_001747885.1:n.6172G=
XR_001747886.1:n.6113G=
XR_001747887.1:n.6158G=
NM_000260.4:c.6093G= MANE Select NP_000251.3:p.Arg2031=
NM_001127180.2:c.5979G= NP_001120652.1:p.Arg1993=
NM_001369365.1:c.5946G= NP_001356294.1:p.Arg1982=