Canonical Allele Identifier: CA1984127876
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77207360G= , CM000673.2:g.77207360G= GRCh38
NC_000011.9:g.76918405G= , CM000673.1:g.76918405G= GRCh37
NC_000011.8:g.76596053G= NCBI36
NG_009086.1:g.84096G=
NG_009086.2:g.84115G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.5814G= MANE Select ENSP00000386331.3:p.Lys1938=
ENST00000670577.1:c.3641G=
ENST00000409619.6:c.5667G= ENSP00000386635.2:p.Lys1889=
ENST00000409709.7:c.5814G= ENSP00000386331.3:p.Lys1938=
ENST00000458169.2:c.3240G= ENSP00000417017.2:p.Lys1080=
ENST00000458637.6:c.5700G= ENSP00000392185.2:p.Lys1900=
ENST00000481328.7:n.3350G=
ENST00000605744.1:n.728G=
NM_000260.3:c.5814G= NP_000251.3:p.Lys1938=
NM_001127180.1:c.5700G= NP_001120652.1:p.Lys1900=
XM_005274012.2:c.5697G= XP_005274069.1:p.Lys1899=
XM_006718558.2:c.5805G= XP_006718621.1:p.Lys1935=
XM_006718559.2:c.5700G= XP_006718622.1:p.Lys1900=
XM_006718560.2:c.5697G= XP_006718623.1:p.Lys1899=
XM_006718561.2:c.5700G= XP_006718624.1:p.Lys1900=
XM_011545044.1:c.5814G= XP_011543346.1:p.Lys1938=
XM_011545045.1:c.5808G= XP_011543347.1:p.Lys1936=
XM_011545046.1:c.5781G= XP_011543348.1:p.Lys1927=
XM_011545047.1:c.5718G= XP_011543349.1:p.Lys1906=
XM_011545048.1:c.5589G= XP_011543350.1:p.Lys1863=
XM_011545049.1:c.5577G= XP_011543351.1:p.Lys1859=
XM_011545050.1:c.5550G= XP_011543352.1:p.Lys1850=
XM_011545051.1:c.5814G= XP_011543353.1:p.Lys1938=
XR_949938.1:n.6134G=
XR_949941.1:n.6134G=
XM_011545044.2:c.5814G= XP_011543346.1:p.Lys1938=
XM_011545046.2:c.5904G= XP_011543348.2:p.Lys1968=
XM_011545050.2:c.5550G= XP_011543352.1:p.Lys1850=
XM_017017778.1:c.5898G= XP_016873267.1:p.Lys1966=
XM_017017779.1:c.5895G= XP_016873268.1:p.Lys1965=
XM_017017780.1:c.5904G= XP_016873269.1:p.Lys1968=
XM_017017781.1:c.5808G= XP_016873270.1:p.Lys1936=
XM_017017782.1:c.5790G= XP_016873271.1:p.Lys1930=
XM_017017783.1:c.5787G= XP_016873272.1:p.Lys1929=
XM_017017784.1:c.5787G= XP_016873273.1:p.Lys1929=
XM_017017785.1:c.5667G= XP_016873274.1:p.Lys1889=
XM_017017786.1:c.5904G= XP_016873275.1:p.Lys1968=
XM_017017788.1:c.5790G= XP_016873277.1:p.Lys1930=
XR_001747885.1:n.5919G=
XR_001747886.1:n.5834G=
XR_001747887.1:n.5905G=
NM_000260.4:c.5814G= MANE Select NP_000251.3:p.Lys1938=
NM_001127180.2:c.5700G= NP_001120652.1:p.Lys1900=
NM_001369365.1:c.5667G= NP_001356294.1:p.Lys1889=