Canonical Allele Identifier: CA1803212133

Gene: TMEM67

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93758887_93758889delinsCTG , CM000670.2:g.93758887_93758889delinsCTG	GRCh38
NC_000008.10:g.94771115_94771117delinsCTG , CM000670.1:g.94771115_94771117delinsCTG	GRCh37
NC_000008.9:g.94840291_94840293delinsCTG	NCBI36
NG_009190.1:g.9044_9046delinsCTG , LRG_688:g.9044_9046delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.406+311_406+313delinsCTG	ENSP00000314488.4:n.406+311_406+313delinsCTG
ENST00000409623.8:c.406+311_406+313delinsCTG	ENSP00000386966.4:n.406+311_406+313delinsCTG
ENST00000452276.6:c.406+311_406+313delinsCTG	ENSP00000388671.2:n.406+311_406+313delinsCTG
ENST00000453906.6:c.406+311_406+313delinsCTG	ENSP00000403035.2:n.406+311_406+313delinsCTG
ENST00000520680.2:c.406+311_406+313delinsCTG	ENSP00000428785.2:n.406+311_406+313delinsCTG
ENST00000521065.2:c.406+311_406+313delinsCTG	ENSP00000427947.2:n.406+311_406+313delinsCTG
ENST00000521517.6:c.406+311_406+313delinsCTG	ENSP00000430740.2:n.406+311_406+313delinsCTG
ENST00000681998.1:c.406+311_406+313delinsCTG	ENSP00000506773.1:n.406+311_406+313delinsCTG
ENST00000682036.1:c.406+311_406+313delinsCTG	ENSP00000508390.1:n.406+311_406+313delinsCTG
ENST00000682577.1:c.406+311_406+313delinsCTG	ENSP00000506963.1:n.406+311_406+313delinsCTG
ENST00000682624.1:c.*50+311_*50+313delinsCTG	ENSP00000508343.1:n.*50+311_*50+313delinsCTG
ENST00000682700.1:c.406+311_406+313delinsCTG	ENSP00000507627.1:n.406+311_406+313delinsCTG
ENST00000682804.1:n.299+311_299+313delinsCTG
ENST00000682837.1:c.406+311_406+313delinsCTG	ENSP00000507920.1:n.406+311_406+313delinsCTG
ENST00000682935.1:n.406+311_406+313delinsCTG
ENST00000682984.1:c.312+3021_312+3023delinsCTG	ENSP00000507209.1:n.312+3021_312+3023delinsCTG
ENST00000683078.1:c.406+311_406+313delinsCTG	ENSP00000506796.1:n.406+311_406+313delinsCTG
ENST00000683223.1:c.317+311_317+313delinsCTG	ENSP00000507685.1:n.317+311_317+313delinsCTG
ENST00000683238.1:n.227+311_227+313delinsCTG
ENST00000683249.1:n.427+311_427+313delinsCTG
ENST00000683336.1:c.406+311_406+313delinsCTG	ENSP00000507695.1:n.406+311_406+313delinsCTG
ENST00000683362.1:c.312+3021_312+3023delinsCTG	ENSP00000506985.1:n.312+3021_312+3023delinsCTG
ENST00000683850.1:n.329+311_329+313delinsCTG
ENST00000683919.1:c.406+311_406+313delinsCTG	ENSP00000507617.1:n.406+311_406+313delinsCTG
ENST00000683953.1:c.317+311_317+313delinsCTG	ENSP00000508375.1:n.317+311_317+313delinsCTG
ENST00000684023.1:c.406+311_406+313delinsCTG	ENSP00000507461.1:n.406+311_406+313delinsCTG
ENST00000684064.1:c.97+311_97+313delinsCTG	ENSP00000508192.1:n.97+311_97+313delinsCTG
ENST00000684089.1:n.396+311_396+313delinsCTG
ENST00000684149.1:c.406+311_406+313delinsCTG	ENSP00000507943.1:n.406+311_406+313delinsCTG
ENST00000684416.1:n.231+311_231+313delinsCTG
ENST00000684540.1:c.406+311_406+313delinsCTG	ENSP00000507987.1:n.406+311_406+313delinsCTG
ENST00000684733.1:n.652_654delinsCTG
ENST00000453321.8:c.406+311_406+313delinsCTG MANE Select	ENSP00000389998.3:n.406+311_406+313delinsCTG
ENST00000323130.7:c.376+311_376+313delinsCTG	ENSP00000314488.3:n.376+311_376+313delinsCTG
ENST00000409623.7:c.29+311_29+313delinsCTG	ENSP00000386966.3:n.29+311_29+313delinsCTG
ENST00000452276.5:c.97+311_97+313delinsCTG	ENSP00000388671.1:n.97+311_97+313delinsCTG
ENST00000453321.7:c.406+311_406+313delinsCTG	ENSP00000389998.3:n.406+311_406+313delinsCTG
ENST00000453906.5:c.406+311_406+313delinsCTG	ENSP00000403035.1:n.406+311_406+313delinsCTG
ENST00000455946.5:c.406+311_406+313delinsCTG	ENSP00000416339.1:n.406+311_406+313delinsCTG
ENST00000474944.5:n.426+311_426+313delinsCTG
ENST00000475305.1:n.726_728delinsCTG
ENST00000498673.5:c.-75+311_-75+313delinsCTG	ENSP00000430232.1:n.-75+311_-75+313delinsCTG
ENST00000518319.5:c.-114+311_-114+313delinsCTG	ENSP00000430289.1:n.-114+311_-114+313delinsCTG
ENST00000521065.1:c.312+311_312+313delinsCTG
ENST00000521222.5:c.*42+311_*42+313delinsCTG	ENSP00000429925.1:n.*42+311_*42+313delinsCTG
ENST00000521517.5:c.398+311_398+313delinsCTG
NM_001142301.1:c.29+311_29+313delinsCTG , LRG_688t2:c.29+311_29+313delinsCTG	NP_001135773.1:n.29+311_29+313delinsCTG
NM_153704.5:c.406+311_406+313delinsCTG , LRG_688t1:c.406+311_406+313delinsCTG	NP_714915.3:n.406+311_406+313delinsCTG
NR_024522.1:n.477+311_477+313delinsCTG
XM_006716686.2:c.103+311_103+313delinsCTG	XP_006716749.1:n.103+311_103+313delinsCTG
XM_011517363.1:c.406+311_406+313delinsCTG	XP_011515665.1:n.406+311_406+313delinsCTG
XR_428387.1:n.464+311_464+313delinsCTG
XR_928360.1:n.464+311_464+313delinsCTG
XR_928361.1:n.464+311_464+313delinsCTG
XR_928362.1:n.464+311_464+313delinsCTG
XM_006716686.4:c.103+311_103+313delinsCTG	XP_006716749.1:n.103+311_103+313delinsCTG
XM_011517363.3:c.406+311_406+313delinsCTG	XP_011515665.1:n.406+311_406+313delinsCTG
XM_024447326.1:c.-4+311_-4+313delinsCTG	XP_024303094.1:n.-4+311_-4+313delinsCTG
XR_001745619.2:n.447+311_447+313delinsCTG
XR_428387.2:n.447+311_447+313delinsCTG
XR_928360.3:n.447+311_447+313delinsCTG
XR_928362.3:n.447+311_447+313delinsCTG
NM_153704.6:c.406+311_406+313delinsCTG MANE Select	NP_714915.3:n.406+311_406+313delinsCTG
NR_024522.2:n.427+311_427+313delinsCTG