Canonical Allele Identifier: CA1803212096

Gene: TMEM67

Linked Data

• dbSNP Id: rs1812693264

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93758814_93758815insC , CM000670.2:g.93758814_93758815insC	GRCh38
NC_000008.10:g.94771042_94771043insC , CM000670.1:g.94771042_94771043insC	GRCh37
NC_000008.9:g.94840218_94840219insC	NCBI36
NG_009190.1:g.8971_8972insC , LRG_688:g.8971_8972insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.406+238_406+239insC	ENSP00000314488.4:n.406+238_406+239insC
ENST00000409623.8:c.406+238_406+239insC	ENSP00000386966.4:n.406+238_406+239insC
ENST00000452276.6:c.406+238_406+239insC	ENSP00000388671.2:n.406+238_406+239insC
ENST00000453906.6:c.406+238_406+239insC	ENSP00000403035.2:n.406+238_406+239insC
ENST00000520680.2:c.406+238_406+239insC	ENSP00000428785.2:n.406+238_406+239insC
ENST00000521065.2:c.406+238_406+239insC	ENSP00000427947.2:n.406+238_406+239insC
ENST00000521517.6:c.406+238_406+239insC	ENSP00000430740.2:n.406+238_406+239insC
ENST00000681998.1:c.406+238_406+239insC	ENSP00000506773.1:n.406+238_406+239insC
ENST00000682036.1:c.406+238_406+239insC	ENSP00000508390.1:n.406+238_406+239insC
ENST00000682577.1:c.406+238_406+239insC	ENSP00000506963.1:n.406+238_406+239insC
ENST00000682624.1:c.*50+238_*50+239insC	ENSP00000508343.1:n.*50+238_*50+239insC
ENST00000682700.1:c.406+238_406+239insC	ENSP00000507627.1:n.406+238_406+239insC
ENST00000682804.1:n.299+238_299+239insC
ENST00000682837.1:c.406+238_406+239insC	ENSP00000507920.1:n.406+238_406+239insC
ENST00000682935.1:n.406+238_406+239insC
ENST00000682984.1:c.312+2948_312+2949insC	ENSP00000507209.1:n.312+2948_312+2949insC
ENST00000683078.1:c.406+238_406+239insC	ENSP00000506796.1:n.406+238_406+239insC
ENST00000683223.1:c.317+238_317+239insC	ENSP00000507685.1:n.317+238_317+239insC
ENST00000683238.1:n.227+238_227+239insC
ENST00000683249.1:n.427+238_427+239insC
ENST00000683336.1:c.406+238_406+239insC	ENSP00000507695.1:n.406+238_406+239insC
ENST00000683362.1:c.312+2948_312+2949insC	ENSP00000506985.1:n.312+2948_312+2949insC
ENST00000683850.1:n.329+238_329+239insC
ENST00000683919.1:c.406+238_406+239insC	ENSP00000507617.1:n.406+238_406+239insC
ENST00000683953.1:c.317+238_317+239insC	ENSP00000508375.1:n.317+238_317+239insC
ENST00000684023.1:c.406+238_406+239insC	ENSP00000507461.1:n.406+238_406+239insC
ENST00000684064.1:c.97+238_97+239insC	ENSP00000508192.1:n.97+238_97+239insC
ENST00000684089.1:n.396+238_396+239insC
ENST00000684149.1:c.406+238_406+239insC	ENSP00000507943.1:n.406+238_406+239insC
ENST00000684416.1:n.231+238_231+239insC
ENST00000684540.1:c.406+238_406+239insC	ENSP00000507987.1:n.406+238_406+239insC
ENST00000684733.1:n.579_580insC
ENST00000453321.8:c.406+238_406+239insC MANE Select	ENSP00000389998.3:n.406+238_406+239insC
ENST00000323130.7:c.376+238_376+239insC	ENSP00000314488.3:n.376+238_376+239insC
ENST00000409623.7:c.29+238_29+239insC	ENSP00000386966.3:n.29+238_29+239insC
ENST00000452276.5:c.97+238_97+239insC	ENSP00000388671.1:n.97+238_97+239insC
ENST00000453321.7:c.406+238_406+239insC	ENSP00000389998.3:n.406+238_406+239insC
ENST00000453906.5:c.406+238_406+239insC	ENSP00000403035.1:n.406+238_406+239insC
ENST00000455946.5:c.406+238_406+239insC	ENSP00000416339.1:n.406+238_406+239insC
ENST00000474944.5:n.426+238_426+239insC
ENST00000475305.1:n.653_654insC
ENST00000498673.5:c.-75+238_-75+239insC	ENSP00000430232.1:n.-75+238_-75+239insC
ENST00000518319.5:c.-114+238_-114+239insC	ENSP00000430289.1:n.-114+238_-114+239insC
ENST00000521065.1:c.312+238_312+239insC
ENST00000521222.5:c.*42+238_*42+239insC	ENSP00000429925.1:n.*42+238_*42+239insC
ENST00000521517.5:c.398+238_398+239insC
NM_001142301.1:c.29+238_29+239insC , LRG_688t2:c.29+238_29+239insC	NP_001135773.1:n.29+238_29+239insC
NM_153704.5:c.406+238_406+239insC , LRG_688t1:c.406+238_406+239insC	NP_714915.3:n.406+238_406+239insC
NR_024522.1:n.477+238_477+239insC
XM_006716686.2:c.103+238_103+239insC	XP_006716749.1:n.103+238_103+239insC
XM_011517363.1:c.406+238_406+239insC	XP_011515665.1:n.406+238_406+239insC
XR_428387.1:n.464+238_464+239insC
XR_928360.1:n.464+238_464+239insC
XR_928361.1:n.464+238_464+239insC
XR_928362.1:n.464+238_464+239insC
XM_006716686.4:c.103+238_103+239insC	XP_006716749.1:n.103+238_103+239insC
XM_011517363.3:c.406+238_406+239insC	XP_011515665.1:n.406+238_406+239insC
XM_024447326.1:c.-4+238_-4+239insC	XP_024303094.1:n.-4+238_-4+239insC
XR_001745619.2:n.447+238_447+239insC
XR_428387.2:n.447+238_447+239insC
XR_928360.3:n.447+238_447+239insC
XR_928362.3:n.447+238_447+239insC
NM_153704.6:c.406+238_406+239insC MANE Select	NP_714915.3:n.406+238_406+239insC
NR_024522.2:n.427+238_427+239insC