Canonical Allele Identifier: CA278695
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43301
ClinVar RCV Id: RCV000036206
dbSNP Id: rs111033238

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77156771del , CM000673.2:g.77156771del GRCh38
NC_000011.9:g.76867817del , CM000673.1:g.76867817del GRCh37
NC_000011.8:g.76545465del NCBI36
NG_009086.1:g.33508del
NG_009086.2:g.33526del

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.582del MANE Select ENSP00000386331.3:p.Ile195PhefsTer?
ENST00000409619.6:c.549del ENSP00000386635.2:p.Ile184PhefsTer?
ENST00000409709.7:c.582del ENSP00000386331.3:p.Ile195PhefsTer?
ENST00000409893.5:c.582del ENSP00000386689.1:p.Ile195PhefsTer?
ENST00000458637.6:c.582del ENSP00000392185.2:p.Ile195PhefsTer?
ENST00000620575.4:c.582del ENSP00000477640.1:p.Ile195PhefsTer?
NM_000260.3:c.582del NP_000251.3:p.Ile195PhefsTer?
NM_001127179.2:c.582del NP_001120651.2:p.Ile195PhefsTer?
NM_001127180.1:c.582del NP_001120652.1:p.Ile195PhefsTer?
XM_005274012.2:c.582del XP_005274069.1:p.Ile195PhefsTer?
XM_006718558.2:c.582del XP_006718621.1:p.Ile195PhefsTer?
XM_006718559.2:c.582del XP_006718622.1:p.Ile195PhefsTer?
XM_006718560.2:c.582del XP_006718623.1:p.Ile195PhefsTer?
XM_006718561.2:c.582del XP_006718624.1:p.Ile195PhefsTer?
XM_011545044.1:c.582del XP_011543346.1:p.Ile195PhefsTer?
XM_011545045.1:c.582del XP_011543347.1:p.Ile195PhefsTer?
XM_011545046.1:c.549del XP_011543348.1:p.Ile184PhefsTer?
XM_011545047.1:c.582del XP_011543349.1:p.Ile195PhefsTer?
XM_011545048.1:c.582del XP_011543350.1:p.Ile195PhefsTer?
XM_011545049.1:c.582del XP_011543351.1:p.Ile195PhefsTer?
XM_011545050.1:c.324del XP_011543352.1:p.Ile109PhefsTer?
XM_011545051.1:c.582del XP_011543353.1:p.Ile195PhefsTer?
XM_011545052.1:c.582del XP_011543354.1:p.Ile195PhefsTer?
XR_949938.1:n.902del
XR_949941.1:n.902del
XR_949942.1:n.904del
XR_949943.1:n.904del
XM_011545044.2:c.582del XP_011543346.1:p.Ile195PhefsTer?
XM_011545046.2:c.672del XP_011543348.2:p.Ile225PhefsTer?
XM_011545050.2:c.324del XP_011543352.1:p.Ile109PhefsTer?
XM_017017778.1:c.672del XP_016873267.1:p.Ile225PhefsTer?
XM_017017779.1:c.672del XP_016873268.1:p.Ile225PhefsTer?
XM_017017780.1:c.672del XP_016873269.1:p.Ile225PhefsTer?
XM_017017781.1:c.672del XP_016873270.1:p.Ile225PhefsTer?
XM_017017782.1:c.672del XP_016873271.1:p.Ile225PhefsTer?
XM_017017783.1:c.672del XP_016873272.1:p.Ile225PhefsTer?
XM_017017784.1:c.672del XP_016873273.1:p.Ile225PhefsTer?
XM_017017785.1:c.672del XP_016873274.1:p.Ile225PhefsTer?
XM_017017786.1:c.672del XP_016873275.1:p.Ile225PhefsTer?
XM_017017787.1:c.672del XP_016873276.1:p.Ile225PhefsTer?
XM_017017788.1:c.672del XP_016873277.1:p.Ile225PhefsTer?
XR_001747885.1:n.687del
XR_001747886.1:n.687del
XR_001747887.1:n.687del
XR_001747888.1:n.687del
XR_001747889.1:n.687del
NM_000260.4:c.582del MANE Select NP_000251.3:p.Ile195PhefsTer?
NM_001127180.2:c.582del NP_001120652.1:p.Ile195PhefsTer?
NM_001369365.1:c.549del NP_001356294.1:p.Ile184PhefsTer?