Canonical Allele Identifier: CA16043874
Gene: MYO7A HGNC NCBI

Linked Data

dbSNP Id: rs1057519225

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77147802_77147803dup , CM000673.2:g.77147802_77147803dup GRCh38
NC_000011.9:g.76858848_76858849dup , CM000673.1:g.76858848_76858849dup GRCh37
NC_000011.8:g.76536496_76536497dup NCBI36
NG_009086.1:g.24539_24540dup
NG_009086.2:g.24557_24558dup

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.137_138dup MANE Select ENSP00000386331.3:p.Trp47ThrfsTer25
ENST00000409619.6:c.104_105dup ENSP00000386635.2:p.Trp36ThrfsTer25
ENST00000409709.7:c.137_138dup ENSP00000386331.3:p.Trp47ThrfsTer25
ENST00000409893.5:c.137_138dup ENSP00000386689.1:p.Trp47ThrfsTer25
ENST00000458637.6:c.137_138dup ENSP00000392185.2:p.Trp47ThrfsTer25
ENST00000620575.4:c.137_138dup ENSP00000477640.1:p.Trp47ThrfsTer25
NM_000260.3:c.137_138dup NP_000251.3:p.Trp47ThrfsTer25
NM_001127179.2:c.137_138dup NP_001120651.2:p.Trp47ThrfsTer25
NM_001127180.1:c.137_138dup NP_001120652.1:p.Trp47ThrfsTer25
XM_005274012.2:c.137_138dup XP_005274069.1:p.Trp47ThrfsTer25
XM_006718558.2:c.137_138dup XP_006718621.1:p.Trp47ThrfsTer25
XM_006718559.2:c.137_138dup XP_006718622.1:p.Trp47ThrfsTer25
XM_006718560.2:c.137_138dup XP_006718623.1:p.Trp47ThrfsTer25
XM_006718561.2:c.137_138dup XP_006718624.1:p.Trp47ThrfsTer25
XM_011545044.1:c.137_138dup XP_011543346.1:p.Trp47ThrfsTer25
XM_011545045.1:c.137_138dup XP_011543347.1:p.Trp47ThrfsTer25
XM_011545046.1:c.104_105dup XP_011543348.1:p.Trp36ThrfsTer25
XM_011545047.1:c.137_138dup XP_011543349.1:p.Trp47ThrfsTer25
XM_011545048.1:c.137_138dup XP_011543350.1:p.Trp47ThrfsTer25
XM_011545049.1:c.137_138dup XP_011543351.1:p.Trp47ThrfsTer25
XM_011545051.1:c.137_138dup XP_011543353.1:p.Trp47ThrfsTer25
XM_011545052.1:c.137_138dup XP_011543354.1:p.Trp47ThrfsTer25
XR_949938.1:n.457_458dup
XR_949941.1:n.457_458dup
XR_949942.1:n.459_460dup
XR_949943.1:n.459_460dup
XM_011545044.2:c.137_138dup XP_011543346.1:p.Trp47ThrfsTer25
XM_011545046.2:c.227_228dup XP_011543348.2:p.Trp77ThrfsTer25
XM_017017778.1:c.227_228dup XP_016873267.1:p.Trp77ThrfsTer25
XM_017017779.1:c.227_228dup XP_016873268.1:p.Trp77ThrfsTer25
XM_017017780.1:c.227_228dup XP_016873269.1:p.Trp77ThrfsTer25
XM_017017781.1:c.227_228dup XP_016873270.1:p.Trp77ThrfsTer25
XM_017017782.1:c.227_228dup XP_016873271.1:p.Trp77ThrfsTer25
XM_017017783.1:c.227_228dup XP_016873272.1:p.Trp77ThrfsTer25
XM_017017784.1:c.227_228dup XP_016873273.1:p.Trp77ThrfsTer25
XM_017017785.1:c.227_228dup XP_016873274.1:p.Trp77ThrfsTer25
XM_017017786.1:c.227_228dup XP_016873275.1:p.Trp77ThrfsTer25
XM_017017787.1:c.227_228dup XP_016873276.1:p.Trp77ThrfsTer25
XM_017017788.1:c.227_228dup XP_016873277.1:p.Trp77ThrfsTer25
XR_001747885.1:n.242_243dup
XR_001747886.1:n.242_243dup
XR_001747887.1:n.242_243dup
XR_001747888.1:n.242_243dup
XR_001747889.1:n.242_243dup
NM_000260.4:c.137_138dup MANE Select NP_000251.3:p.Trp47ThrfsTer25
NM_001127180.2:c.137_138dup NP_001120652.1:p.Trp47ThrfsTer25
NM_001369365.1:c.104_105dup NP_001356294.1:p.Trp36ThrfsTer25