Canonical Allele Identifier: CA1984122759
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77199712C= , CM000673.2:g.77199712C= GRCh38
NC_000011.9:g.76910757C= , CM000673.1:g.76910757C= GRCh37
NC_000011.8:g.76588405C= NCBI36
NG_009086.1:g.76448C=
NG_009086.2:g.76467C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.4746C= MANE Select ENSP00000386331.3:p.Phe1582=
ENST00000670577.1:c.2587C=
ENST00000409619.6:c.4599C= ENSP00000386635.2:p.Phe1533=
ENST00000409709.7:c.4746C= ENSP00000386331.3:p.Phe1582=
ENST00000458169.2:c.2175C= ENSP00000417017.2:p.Phe725=
ENST00000458637.6:c.4632C= ENSP00000392185.2:p.Phe1544=
ENST00000481328.7:n.2285C=
NM_000260.3:c.4746C= NP_000251.3:p.Phe1582=
NM_001127180.1:c.4632C= NP_001120652.1:p.Phe1544=
XM_005274012.2:c.4632C= XP_005274069.1:p.Phe1544=
XM_006718558.2:c.4740C= XP_006718621.1:p.Phe1580=
XM_006718559.2:c.4632C= XP_006718622.1:p.Phe1544=
XM_006718560.2:c.4632C= XP_006718623.1:p.Phe1544=
XM_006718561.2:c.4632C= XP_006718624.1:p.Phe1544=
XM_011545044.1:c.4746C= XP_011543346.1:p.Phe1582=
XM_011545045.1:c.4740C= XP_011543347.1:p.Phe1580=
XM_011545046.1:c.4713C= XP_011543348.1:p.Phe1571=
XM_011545047.1:c.4650C= XP_011543349.1:p.Phe1550=
XM_011545048.1:c.4521C= XP_011543350.1:p.Phe1507=
XM_011545049.1:c.4509C= XP_011543351.1:p.Phe1503=
XM_011545050.1:c.4482C= XP_011543352.1:p.Phe1494=
XM_011545051.1:c.4746C= XP_011543353.1:p.Phe1582=
XM_011545052.1:c.4746C= XP_011543354.1:p.Phe1582=
XR_949938.1:n.5066C=
XR_949941.1:n.5066C=
XR_949942.1:n.5068C=
XM_011545044.2:c.4746C= XP_011543346.1:p.Phe1582=
XM_011545046.2:c.4836C= XP_011543348.2:p.Phe1612=
XM_011545050.2:c.4482C= XP_011543352.1:p.Phe1494=
XM_017017778.1:c.4830C= XP_016873267.1:p.Phe1610=
XM_017017779.1:c.4830C= XP_016873268.1:p.Phe1610=
XM_017017780.1:c.4836C= XP_016873269.1:p.Phe1612=
XM_017017781.1:c.4740C= XP_016873270.1:p.Phe1580=
XM_017017782.1:c.4722C= XP_016873271.1:p.Phe1574=
XM_017017783.1:c.4722C= XP_016873272.1:p.Phe1574=
XM_017017784.1:c.4722C= XP_016873273.1:p.Phe1574=
XM_017017785.1:c.4599C= XP_016873274.1:p.Phe1533=
XM_017017786.1:c.4836C= XP_016873275.1:p.Phe1612=
XM_017017788.1:c.4722C= XP_016873277.1:p.Phe1574=
XR_001747885.1:n.4851C=
XR_001747886.1:n.4851C=
XR_001747887.1:n.4851C=
XR_001747888.1:n.4851C=
NM_000260.4:c.4746C= MANE Select NP_000251.3:p.Phe1582=
NM_001127180.2:c.4632C= NP_001120652.1:p.Phe1544=
NM_001369365.1:c.4599C= NP_001356294.1:p.Phe1533=