Canonical Allele Identifier: CA2781323242

Gene: TMEM67

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93758649_93758661del , CM000670.2:g.93758649_93758661del	GRCh38
NC_000008.10:g.94770877_94770889del , CM000670.1:g.94770877_94770889del	GRCh37
NC_000008.9:g.94840053_94840065del	NCBI36
NG_009190.1:g.8806_8818del , LRG_688:g.8806_8818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.406+73_406+85del	ENSP00000314488.4:n.406+73_406+85del
ENST00000409623.8:c.406+73_406+85del	ENSP00000386966.4:n.406+73_406+85del
ENST00000452276.6:c.406+73_406+85del	ENSP00000388671.2:n.406+73_406+85del
ENST00000453906.6:c.406+73_406+85del	ENSP00000403035.2:n.406+73_406+85del
ENST00000520680.2:c.406+73_406+85del	ENSP00000428785.2:n.406+73_406+85del
ENST00000521065.2:c.406+73_406+85del	ENSP00000427947.2:n.406+73_406+85del
ENST00000521517.6:c.406+73_406+85del	ENSP00000430740.2:n.406+73_406+85del
ENST00000681998.1:c.406+73_406+85del	ENSP00000506773.1:n.406+73_406+85del
ENST00000682036.1:c.406+73_406+85del	ENSP00000508390.1:n.406+73_406+85del
ENST00000682577.1:c.406+73_406+85del	ENSP00000506963.1:n.406+73_406+85del
ENST00000682624.1:c.*50+73_*50+85del	ENSP00000508343.1:n.*50+73_*50+85del
ENST00000682700.1:c.406+73_406+85del	ENSP00000507627.1:n.406+73_406+85del
ENST00000682804.1:n.299+73_299+85del
ENST00000682837.1:c.406+73_406+85del	ENSP00000507920.1:n.406+73_406+85del
ENST00000682935.1:n.406+73_406+85del
ENST00000682984.1:c.312+2783_312+2795del	ENSP00000507209.1:n.312+2783_312+2795del
ENST00000683078.1:c.406+73_406+85del	ENSP00000506796.1:n.406+73_406+85del
ENST00000683223.1:c.317+73_317+85del	ENSP00000507685.1:n.317+73_317+85del
ENST00000683238.1:n.227+73_227+85del
ENST00000683249.1:n.427+73_427+85del
ENST00000683336.1:c.406+73_406+85del	ENSP00000507695.1:n.406+73_406+85del
ENST00000683362.1:c.312+2783_312+2795del	ENSP00000506985.1:n.312+2783_312+2795del
ENST00000683850.1:n.329+73_329+85del
ENST00000683919.1:c.406+73_406+85del	ENSP00000507617.1:n.406+73_406+85del
ENST00000683953.1:c.317+73_317+85del	ENSP00000508375.1:n.317+73_317+85del
ENST00000684023.1:c.406+73_406+85del	ENSP00000507461.1:n.406+73_406+85del
ENST00000684064.1:c.97+73_97+85del	ENSP00000508192.1:n.97+73_97+85del
ENST00000684089.1:n.396+73_396+85del
ENST00000684149.1:c.406+73_406+85del	ENSP00000507943.1:n.406+73_406+85del
ENST00000684416.1:n.231+73_231+85del
ENST00000684540.1:c.406+73_406+85del	ENSP00000507987.1:n.406+73_406+85del
ENST00000684733.1:n.414_426del
ENST00000453321.8:c.406+73_406+85del MANE Select	ENSP00000389998.3:n.406+73_406+85del
ENST00000323130.7:c.376+73_376+85del	ENSP00000314488.3:n.376+73_376+85del
ENST00000409623.7:c.29+73_29+85del	ENSP00000386966.3:n.29+73_29+85del
ENST00000452276.5:c.97+73_97+85del	ENSP00000388671.1:n.97+73_97+85del
ENST00000453321.7:c.406+73_406+85del	ENSP00000389998.3:n.406+73_406+85del
ENST00000453906.5:c.406+73_406+85del	ENSP00000403035.1:n.406+73_406+85del
ENST00000455946.5:c.406+73_406+85del	ENSP00000416339.1:n.406+73_406+85del
ENST00000474944.5:n.426+73_426+85del
ENST00000475305.1:n.488_500del
ENST00000498673.5:c.-75+73_-75+85del	ENSP00000430232.1:n.-75+73_-75+85del
ENST00000518319.5:c.-114+73_-114+85del	ENSP00000430289.1:n.-114+73_-114+85del
ENST00000521065.1:c.312+73_312+85del
ENST00000521222.5:c.*42+73_*42+85del	ENSP00000429925.1:n.*42+73_*42+85del
ENST00000521517.5:c.398+73_398+85del
NM_001142301.1:c.29+73_29+85del , LRG_688t2:c.29+73_29+85del	NP_001135773.1:n.29+73_29+85del
NM_153704.5:c.406+73_406+85del , LRG_688t1:c.406+73_406+85del	NP_714915.3:n.406+73_406+85del
NR_024522.1:n.477+73_477+85del
XM_006716686.2:c.103+73_103+85del	XP_006716749.1:n.103+73_103+85del
XM_011517363.1:c.406+73_406+85del	XP_011515665.1:n.406+73_406+85del
XR_428387.1:n.464+73_464+85del
XR_928360.1:n.464+73_464+85del
XR_928361.1:n.464+73_464+85del
XR_928362.1:n.464+73_464+85del
XM_006716686.4:c.103+73_103+85del	XP_006716749.1:n.103+73_103+85del
XM_011517363.3:c.406+73_406+85del	XP_011515665.1:n.406+73_406+85del
XM_024447326.1:c.-4+73_-4+85del	XP_024303094.1:n.-4+73_-4+85del
XR_001745619.2:n.447+73_447+85del
XR_428387.2:n.447+73_447+85del
XR_928360.3:n.447+73_447+85del
XR_928362.3:n.447+73_447+85del
NM_153704.6:c.406+73_406+85del MANE Select	NP_714915.3:n.406+73_406+85del
NR_024522.2:n.427+73_427+85del