Canonical Allele Identifier: CA381951669
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77202357C>G , CM000673.2:g.77202357C>G GRCh38
NC_000011.9:g.76913402C>G , CM000673.1:g.76913402C>G GRCh37
NC_000011.8:g.76591050C>G NCBI36
NG_009086.1:g.79093C>G
NG_009086.2:g.79112C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000260.4:c.5101C>G MANE Select NP_000251.3:p.Arg1701Gly
ENST00000409709.9:c.5101C>G MANE Select ENSP00000386331.3:p.Arg1701Gly
NM_000260.3:c.5101C>G NP_000251.3:p.Arg1701Gly
NM_001127180.1:c.4987C>G NP_001120652.1:p.Arg1663Gly
NM_001127180.2:c.4987C>G NP_001120652.1:p.Arg1663Gly
NM_001369365.1:c.4954C>G NP_001356294.1:p.Arg1652Gly
ENST00000409619.6:c.4954C>G ENSP00000386635.2:p.Arg1652Gly
ENST00000409709.7:c.5101C>G ENSP00000386331.3:p.Arg1701Gly
ENST00000458169.2:c.2527C>G ENSP00000417017.2:p.Arg843Gly
ENST00000458637.6:c.4987C>G ENSP00000392185.2:p.Arg1663Gly
ENST00000481328.7:n.2637C>G
ENST00000670577.1:c.2942C>G
XM_005274012.2:c.4984C>G XP_005274069.1:p.Arg1662Gly
XM_006718558.2:c.5092C>G XP_006718621.1:p.Arg1698Gly
XM_006718559.2:c.4987C>G XP_006718622.1:p.Arg1663Gly
XM_006718560.2:c.4984C>G XP_006718623.1:p.Arg1662Gly
XM_006718561.2:c.4987C>G XP_006718624.1:p.Arg1663Gly
XM_011545044.1:c.5101C>G XP_011543346.1:p.Arg1701Gly
XM_011545044.2:c.5101C>G XP_011543346.1:p.Arg1701Gly
XM_011545045.1:c.5095C>G XP_011543347.1:p.Arg1699Gly
XM_011545046.1:c.5068C>G XP_011543348.1:p.Arg1690Gly
XM_011545046.2:c.5191C>G XP_011543348.2:p.Arg1731Gly
XM_011545047.1:c.5005C>G XP_011543349.1:p.Arg1669Gly
XM_011545048.1:c.4876C>G XP_011543350.1:p.Arg1626Gly
XM_011545049.1:c.4864C>G XP_011543351.1:p.Arg1622Gly
XM_011545050.1:c.4837C>G XP_011543352.1:p.Arg1613Gly
XM_011545050.2:c.4837C>G XP_011543352.1:p.Arg1613Gly
XM_011545051.1:c.5101C>G XP_011543353.1:p.Arg1701Gly
XM_011545052.1:c.5101C>G XP_011543354.1:p.Arg1701Gly
XM_017017778.1:c.5185C>G XP_016873267.1:p.Arg1729Gly
XM_017017779.1:c.5182C>G XP_016873268.1:p.Arg1728Gly
XM_017017780.1:c.5191C>G XP_016873269.1:p.Arg1731Gly
XM_017017781.1:c.5095C>G XP_016873270.1:p.Arg1699Gly
XM_017017782.1:c.5077C>G XP_016873271.1:p.Arg1693Gly
XM_017017783.1:c.5074C>G XP_016873272.1:p.Arg1692Gly
XM_017017784.1:c.5074C>G XP_016873273.1:p.Arg1692Gly
XM_017017785.1:c.4954C>G XP_016873274.1:p.Arg1652Gly
XM_017017786.1:c.5191C>G XP_016873275.1:p.Arg1731Gly
XM_017017788.1:c.5077C>G XP_016873277.1:p.Arg1693Gly
XR_001747885.1:n.5206C>G
XR_001747886.1:n.5206C>G
XR_001747887.1:n.5206C>G
XR_001747888.1:n.5206C>G
XR_949938.1:n.5421C>G
XR_949941.1:n.5421C>G
XR_949942.1:n.5423C>G