Canonical Allele Identifier: CA1984124428
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77201591A= , CM000673.2:g.77201591A= GRCh38
NC_000011.9:g.76912636A= , CM000673.1:g.76912636A= GRCh37
NC_000011.8:g.76590284A= NCBI36
NG_009086.1:g.78327A=
NG_009086.2:g.78346A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.4996A= MANE Select ENSP00000386331.3:p.Ser1666=
ENST00000670577.1:c.2837A=
ENST00000409619.6:c.4849A= ENSP00000386635.2:p.Ser1617=
ENST00000409709.7:c.4996A= ENSP00000386331.3:p.Ser1666=
ENST00000458169.2:c.2422A= ENSP00000417017.2:p.Ser808=
ENST00000458637.6:c.4882A= ENSP00000392185.2:p.Ser1628=
ENST00000481328.7:n.2532A=
NM_000260.3:c.4996A= NP_000251.3:p.Ser1666=
NM_001127180.1:c.4882A= NP_001120652.1:p.Ser1628=
XM_005274012.2:c.4879A= XP_005274069.1:p.Ser1627=
XM_006718558.2:c.4987A= XP_006718621.1:p.Ser1663=
XM_006718559.2:c.4882A= XP_006718622.1:p.Ser1628=
XM_006718560.2:c.4879A= XP_006718623.1:p.Ser1627=
XM_006718561.2:c.4882A= XP_006718624.1:p.Ser1628=
XM_011545044.1:c.4996A= XP_011543346.1:p.Ser1666=
XM_011545045.1:c.4990A= XP_011543347.1:p.Ser1664=
XM_011545046.1:c.4963A= XP_011543348.1:p.Ser1655=
XM_011545047.1:c.4900A= XP_011543349.1:p.Ser1634=
XM_011545048.1:c.4771A= XP_011543350.1:p.Ser1591=
XM_011545049.1:c.4759A= XP_011543351.1:p.Ser1587=
XM_011545050.1:c.4732A= XP_011543352.1:p.Ser1578=
XM_011545051.1:c.4996A= XP_011543353.1:p.Ser1666=
XM_011545052.1:c.4996A= XP_011543354.1:p.Ser1666=
XR_949938.1:n.5316A=
XR_949941.1:n.5316A=
XR_949942.1:n.5318A=
XM_011545044.2:c.4996A= XP_011543346.1:p.Ser1666=
XM_011545046.2:c.5086A= XP_011543348.2:p.Ser1696=
XM_011545050.2:c.4732A= XP_011543352.1:p.Ser1578=
XM_017017778.1:c.5080A= XP_016873267.1:p.Ser1694=
XM_017017779.1:c.5077A= XP_016873268.1:p.Ser1693=
XM_017017780.1:c.5086A= XP_016873269.1:p.Ser1696=
XM_017017781.1:c.4990A= XP_016873270.1:p.Ser1664=
XM_017017782.1:c.4972A= XP_016873271.1:p.Ser1658=
XM_017017783.1:c.4969A= XP_016873272.1:p.Ser1657=
XM_017017784.1:c.4969A= XP_016873273.1:p.Ser1657=
XM_017017785.1:c.4849A= XP_016873274.1:p.Ser1617=
XM_017017786.1:c.5086A= XP_016873275.1:p.Ser1696=
XM_017017788.1:c.4972A= XP_016873277.1:p.Ser1658=
XR_001747885.1:n.5101A=
XR_001747886.1:n.5101A=
XR_001747887.1:n.5101A=
XR_001747888.1:n.5101A=
NM_000260.4:c.4996A= MANE Select NP_000251.3:p.Ser1666=
NM_001127180.2:c.4882A= NP_001120652.1:p.Ser1628=
NM_001369365.1:c.4849A= NP_001356294.1:p.Ser1617=