Canonical Allele Identifier: CA2687919221

Gene: TMEM67

Linked Data

• gnomAD v4: 8-93765386-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93765391dup , CM000670.2:g.93765391dup	GRCh38
NC_000008.10:g.94777619dup , CM000670.1:g.94777619dup	GRCh37
NC_000008.9:g.94846795dup	NCBI36
NG_009190.1:g.15548dup , LRG_688:g.15548dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.507-15dup	ENSP00000314488.4:n.507-15dup
ENST00000409623.8:c.507-15dup	ENSP00000386966.4:n.507-15dup
ENST00000452276.6:c.507-15dup	ENSP00000388671.2:n.507-15dup
ENST00000453906.6:c.406+6815dup	ENSP00000403035.2:n.406+6815dup
ENST00000520680.2:c.507-15dup	ENSP00000428785.2:n.507-15dup
ENST00000521065.2:c.*224-15dup	ENSP00000427947.2:n.*224-15dup
ENST00000521517.6:c.507-15dup	ENSP00000430740.2:n.507-15dup
ENST00000681998.1:c.507-181dup	ENSP00000506773.1:n.507-181dup
ENST00000682036.1:c.406+6815dup	ENSP00000508390.1:n.406+6815dup
ENST00000682577.1:c.507-181dup	ENSP00000506963.1:n.507-181dup
ENST00000682624.1:c.*151-181dup	ENSP00000508343.1:n.*151-181dup
ENST00000682700.1:c.507-15dup	ENSP00000507627.1:n.507-15dup
ENST00000682804.1:n.400-181dup
ENST00000682837.1:c.406+6815dup	ENSP00000507920.1:n.406+6815dup
ENST00000682935.1:n.1956dup
ENST00000682984.1:c.313-7198dup	ENSP00000507209.1:n.313-7198dup
ENST00000683078.1:c.406+6815dup	ENSP00000506796.1:n.406+6815dup
ENST00000683223.1:c.418-181dup	ENSP00000507685.1:n.418-181dup
ENST00000683238.1:n.1777dup
ENST00000683249.1:n.1977dup
ENST00000683336.1:c.507-181dup	ENSP00000507695.1:n.507-181dup
ENST00000683362.1:c.313-7198dup	ENSP00000506985.1:n.313-7198dup
ENST00000683850.1:n.430-15dup
ENST00000683919.1:c.507-181dup	ENSP00000507617.1:n.507-181dup
ENST00000683953.1:c.418-15dup	ENSP00000508375.1:n.418-15dup
ENST00000684023.1:c.641-15dup	ENSP00000507461.1:n.641-15dup
ENST00000684064.1:c.198-15dup	ENSP00000508192.1:n.198-15dup
ENST00000684089.1:n.1946dup
ENST00000684149.1:c.507-181dup	ENSP00000507943.1:n.507-181dup
ENST00000684416.1:n.466-15dup
ENST00000684540.1:c.507-181dup	ENSP00000507987.1:n.507-181dup
ENST00000453321.8:c.507-15dup MANE Select	ENSP00000389998.3:n.507-15dup
ENST00000323130.7:c.477-15dup	ENSP00000314488.3:n.477-15dup
ENST00000409623.7:c.264-15dup	ENSP00000386966.3:n.264-15dup
ENST00000452276.5:c.198-15dup	ENSP00000388671.1:n.198-15dup
ENST00000453321.7:c.507-15dup	ENSP00000389998.3:n.507-15dup
ENST00000453906.5:c.406+6815dup	ENSP00000403035.1:n.406+6815dup
ENST00000455946.5:c.*179-15dup	ENSP00000416339.1:n.*179-15dup
ENST00000474944.5:n.426+6815dup
ENST00000518319.5:c.27-15dup	ENSP00000430289.1:n.27-15dup
ENST00000521065.1:c.413-15dup
ENST00000521222.5:c.*143-15dup	ENSP00000429925.1:n.*143-15dup
ENST00000521517.5:c.499-181dup
NM_001142301.1:c.264-15dup , LRG_688t2:c.264-15dup	NP_001135773.1:n.264-15dup
NM_153704.5:c.507-15dup , LRG_688t1:c.507-15dup	NP_714915.3:n.507-15dup
NR_024522.1:n.578-15dup
XM_006716686.2:c.204-15dup	XP_006716749.1:n.204-15dup
XM_011517363.1:c.406+6815dup	XP_011515665.1:n.406+6815dup
XR_428387.1:n.565-15dup
XR_928360.1:n.565-15dup
XR_928361.1:n.565-15dup
XR_928362.1:n.565-15dup
XM_006716686.4:c.204-15dup	XP_006716749.1:n.204-15dup
XM_011517363.3:c.406+6815dup	XP_011515665.1:n.406+6815dup
XM_024447326.1:c.-4+6815dup	XP_024303094.1:n.-4+6815dup
XR_001745619.2:n.548-15dup
XR_428387.2:n.548-15dup
XR_928360.3:n.548-15dup
XR_928362.3:n.548-15dup
NM_153704.6:c.507-15dup MANE Select	NP_714915.3:n.507-15dup
NR_024522.2:n.528-15dup