Canonical Allele Identifier: CA475791967
Gene: MYO7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.76922280G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77211235G>A , CM000673.2:g.77211235G>A GRCh38
NC_000011.9:g.76922280G>A , CM000673.1:g.76922280G>A GRCh37
NC_000011.8:g.76599928G>A NCBI36
NG_009086.1:g.87971G>A
NG_009086.2:g.87990G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.6135G>A MANE Select ENSP00000386331.3:p.Lys2045=
ENST00000670577.1:c.3936G>A
ENST00000409619.6:c.5988G>A ENSP00000386635.2:p.Lys1996=
ENST00000409709.7:c.6135G>A ENSP00000386331.3:p.Lys2045=
ENST00000458169.2:c.3561G>A ENSP00000417017.2:p.Lys1187=
ENST00000458637.6:c.6021G>A ENSP00000392185.2:p.Lys2007=
ENST00000481328.7:n.3671G>A
ENST00000526863.2:n.25+324G>A
ENST00000605744.1:n.1602G>A
NM_000260.3:c.6135G>A NP_000251.3:p.Lys2045=
NM_001127180.1:c.6021G>A NP_001120652.1:p.Lys2007=
XM_005274012.2:c.6018G>A XP_005274069.1:p.Lys2006=
XM_006718558.2:c.6126G>A XP_006718621.1:p.Lys2042=
XM_006718559.2:c.6021G>A XP_006718622.1:p.Lys2007=
XM_006718560.2:c.6018G>A XP_006718623.1:p.Lys2006=
XM_006718561.2:c.6021G>A XP_006718624.1:p.Lys2007=
XM_011545044.1:c.6135G>A XP_011543346.1:p.Lys2045=
XM_011545045.1:c.6129G>A XP_011543347.1:p.Lys2043=
XM_011545046.1:c.6102G>A XP_011543348.1:p.Lys2034=
XM_011545047.1:c.6039G>A XP_011543349.1:p.Lys2013=
XM_011545048.1:c.5910G>A XP_011543350.1:p.Lys1970=
XM_011545049.1:c.5898G>A XP_011543351.1:p.Lys1966=
XM_011545050.1:c.5871G>A XP_011543352.1:p.Lys1957=
XM_011545051.1:c.6135G>A XP_011543353.1:p.Lys2045=
XR_949938.1:n.6455G>A
XR_949941.1:n.6429G>A
XM_011545044.2:c.6135G>A XP_011543346.1:p.Lys2045=
XM_011545046.2:c.6225G>A XP_011543348.2:p.Lys2075=
XM_011545050.2:c.5871G>A XP_011543352.1:p.Lys1957=
XM_017017778.1:c.6219G>A XP_016873267.1:p.Lys2073=
XM_017017779.1:c.6216G>A XP_016873268.1:p.Lys2072=
XM_017017780.1:c.6225G>A XP_016873269.1:p.Lys2075=
XM_017017781.1:c.6129G>A XP_016873270.1:p.Lys2043=
XM_017017782.1:c.6111G>A XP_016873271.1:p.Lys2037=
XM_017017783.1:c.6108G>A XP_016873272.1:p.Lys2036=
XM_017017784.1:c.6108G>A XP_016873273.1:p.Lys2036=
XM_017017785.1:c.5988G>A XP_016873274.1:p.Lys1996=
XM_017017786.1:c.6225G>A XP_016873275.1:p.Lys2075=
XM_017017788.1:c.6111G>A XP_016873277.1:p.Lys2037=
XR_001747885.1:n.6214G>A
XR_001747886.1:n.6155G>A
XR_001747887.1:n.6200G>A
NM_000260.4:c.6135G>A MANE Select NP_000251.3:p.Lys2045=
NM_001127180.2:c.6021G>A NP_001120652.1:p.Lys2007=
NM_001369365.1:c.5988G>A NP_001356294.1:p.Lys1996=