Canonical Allele Identifier: CA2781323245
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93758656_93758657del , CM000670.2:g.93758656_93758657del GRCh38
NC_000008.10:g.94770884_94770885del , CM000670.1:g.94770884_94770885del GRCh37
NC_000008.9:g.94840060_94840061del NCBI36
NG_009190.1:g.8813_8814del , LRG_688:g.8813_8814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.406+80_406+81del ENSP00000314488.4:n.406+80_406+81del
ENST00000409623.8:c.406+80_406+81del ENSP00000386966.4:n.406+80_406+81del
ENST00000452276.6:c.406+80_406+81del ENSP00000388671.2:n.406+80_406+81del
ENST00000453906.6:c.406+80_406+81del ENSP00000403035.2:n.406+80_406+81del
ENST00000520680.2:c.406+80_406+81del ENSP00000428785.2:n.406+80_406+81del
ENST00000521065.2:c.406+80_406+81del ENSP00000427947.2:n.406+80_406+81del
ENST00000521517.6:c.406+80_406+81del ENSP00000430740.2:n.406+80_406+81del
ENST00000681998.1:c.406+80_406+81del ENSP00000506773.1:n.406+80_406+81del
ENST00000682036.1:c.406+80_406+81del ENSP00000508390.1:n.406+80_406+81del
ENST00000682577.1:c.406+80_406+81del ENSP00000506963.1:n.406+80_406+81del
ENST00000682624.1:c.*50+80_*50+81del ENSP00000508343.1:n.*50+80_*50+81del
ENST00000682700.1:c.406+80_406+81del ENSP00000507627.1:n.406+80_406+81del
ENST00000682804.1:n.299+80_299+81del
ENST00000682837.1:c.406+80_406+81del ENSP00000507920.1:n.406+80_406+81del
ENST00000682935.1:n.406+80_406+81del
ENST00000682984.1:c.312+2790_312+2791del ENSP00000507209.1:n.312+2790_312+2791del
ENST00000683078.1:c.406+80_406+81del ENSP00000506796.1:n.406+80_406+81del
ENST00000683223.1:c.317+80_317+81del ENSP00000507685.1:n.317+80_317+81del
ENST00000683238.1:n.227+80_227+81del
ENST00000683249.1:n.427+80_427+81del
ENST00000683336.1:c.406+80_406+81del ENSP00000507695.1:n.406+80_406+81del
ENST00000683362.1:c.312+2790_312+2791del ENSP00000506985.1:n.312+2790_312+2791del
ENST00000683850.1:n.329+80_329+81del
ENST00000683919.1:c.406+80_406+81del ENSP00000507617.1:n.406+80_406+81del
ENST00000683953.1:c.317+80_317+81del ENSP00000508375.1:n.317+80_317+81del
ENST00000684023.1:c.406+80_406+81del ENSP00000507461.1:n.406+80_406+81del
ENST00000684064.1:c.97+80_97+81del ENSP00000508192.1:n.97+80_97+81del
ENST00000684089.1:n.396+80_396+81del
ENST00000684149.1:c.406+80_406+81del ENSP00000507943.1:n.406+80_406+81del
ENST00000684416.1:n.231+80_231+81del
ENST00000684540.1:c.406+80_406+81del ENSP00000507987.1:n.406+80_406+81del
ENST00000684733.1:n.421_422del
ENST00000453321.8:c.406+80_406+81del MANE Select ENSP00000389998.3:n.406+80_406+81del
ENST00000323130.7:c.376+80_376+81del ENSP00000314488.3:n.376+80_376+81del
ENST00000409623.7:c.29+80_29+81del ENSP00000386966.3:n.29+80_29+81del
ENST00000452276.5:c.97+80_97+81del ENSP00000388671.1:n.97+80_97+81del
ENST00000453321.7:c.406+80_406+81del ENSP00000389998.3:n.406+80_406+81del
ENST00000453906.5:c.406+80_406+81del ENSP00000403035.1:n.406+80_406+81del
ENST00000455946.5:c.406+80_406+81del ENSP00000416339.1:n.406+80_406+81del
ENST00000474944.5:n.426+80_426+81del
ENST00000475305.1:n.495_496del
ENST00000498673.5:c.-75+80_-75+81del ENSP00000430232.1:n.-75+80_-75+81del
ENST00000518319.5:c.-114+80_-114+81del ENSP00000430289.1:n.-114+80_-114+81del
ENST00000521065.1:c.312+80_312+81del
ENST00000521222.5:c.*42+80_*42+81del ENSP00000429925.1:n.*42+80_*42+81del
ENST00000521517.5:c.398+80_398+81del
NM_001142301.1:c.29+80_29+81del , LRG_688t2:c.29+80_29+81del NP_001135773.1:n.29+80_29+81del
NM_153704.5:c.406+80_406+81del , LRG_688t1:c.406+80_406+81del NP_714915.3:n.406+80_406+81del
NR_024522.1:n.477+80_477+81del
XM_006716686.2:c.103+80_103+81del XP_006716749.1:n.103+80_103+81del
XM_011517363.1:c.406+80_406+81del XP_011515665.1:n.406+80_406+81del
XR_428387.1:n.464+80_464+81del
XR_928360.1:n.464+80_464+81del
XR_928361.1:n.464+80_464+81del
XR_928362.1:n.464+80_464+81del
XM_006716686.4:c.103+80_103+81del XP_006716749.1:n.103+80_103+81del
XM_011517363.3:c.406+80_406+81del XP_011515665.1:n.406+80_406+81del
XM_024447326.1:c.-4+80_-4+81del XP_024303094.1:n.-4+80_-4+81del
XR_001745619.2:n.447+80_447+81del
XR_428387.2:n.447+80_447+81del
XR_928360.3:n.447+80_447+81del
XR_928362.3:n.447+80_447+81del
NM_153704.6:c.406+80_406+81del MANE Select NP_714915.3:n.406+80_406+81del
NR_024522.2:n.427+80_427+81del