Canonical Allele Identifier: CA371685742

Gene: TMEM67

Linked Data

• gnomAD v4: 8-93758487-G-T
• MyVariant Identifiers: chr8:g.94770715G>T (hg19) ; chr8:g.93758487G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93758487G>T , CM000670.2:g.93758487G>T	GRCh38
NC_000008.10:g.94770715G>T , CM000670.1:g.94770715G>T	GRCh37
NC_000008.9:g.94839891G>T	NCBI36
NG_009190.1:g.8644G>T , LRG_688:g.8644G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.317G>T	ENSP00000314488.4:p.Gly106Val
ENST00000409623.8:c.317G>T	ENSP00000386966.4:p.Gly106Val
ENST00000452276.6:c.317G>T	ENSP00000388671.2:p.Gly106Val
ENST00000453906.6:c.317G>T	ENSP00000403035.2:p.Gly106Val
ENST00000520680.2:c.317G>T	ENSP00000428785.2:p.Gly106Val
ENST00000521065.2:c.317G>T	ENSP00000427947.2:p.Gly106Val
ENST00000521517.6:c.317G>T	ENSP00000430740.2:p.Gly106Val
ENST00000681998.1:c.317G>T	ENSP00000506773.1:p.Gly106Val
ENST00000682036.1:c.317G>T	ENSP00000508390.1:p.Gly106Val
ENST00000682577.1:c.317G>T	ENSP00000506963.1:p.Gly106Val
ENST00000682624.1:c.228G>T	ENSP00000508343.1:p.Arg76Ser
ENST00000682700.1:c.317G>T	ENSP00000507627.1:p.Gly106Val
ENST00000682804.1:n.210G>T
ENST00000682837.1:c.317G>T	ENSP00000507920.1:p.Gly106Val
ENST00000682935.1:n.317G>T
ENST00000682984.1:c.312+2621G>T	ENSP00000507209.1:n.312+2621G>T
ENST00000683078.1:c.317G>T	ENSP00000506796.1:p.Gly106Val
ENST00000683223.1:c.228G>T	ENSP00000507685.1:p.Arg76Ser
ENST00000683238.1:n.138G>T
ENST00000683249.1:n.338G>T
ENST00000683336.1:c.317G>T	ENSP00000507695.1:p.Gly106Val
ENST00000683362.1:c.312+2621G>T	ENSP00000506985.1:n.312+2621G>T
ENST00000683850.1:n.240G>T
ENST00000683919.1:c.317G>T	ENSP00000507617.1:p.Gly106Val
ENST00000683953.1:c.228G>T	ENSP00000508375.1:p.Arg76Ser
ENST00000684023.1:c.317G>T	ENSP00000507461.1:p.Gly106Val
ENST00000684064.1:c.8G>T	ENSP00000508192.1:p.Gly3Val
ENST00000684089.1:n.307G>T
ENST00000684149.1:c.317G>T	ENSP00000507943.1:p.Gly106Val
ENST00000684416.1:n.142G>T
ENST00000684540.1:c.317G>T	ENSP00000507987.1:p.Gly106Val
ENST00000684733.1:n.252G>T
ENST00000453321.8:c.317G>T MANE Select	ENSP00000389998.3:p.Gly106Val
ENST00000323130.7:c.287G>T	ENSP00000314488.3:p.Gly96Val
ENST00000409623.7:c.-61G>T	ENSP00000386966.3:n.-61G>T
ENST00000452276.5:c.8G>T	ENSP00000388671.1:p.Gly3Val
ENST00000453321.7:c.317G>T	ENSP00000389998.3:p.Gly106Val
ENST00000453906.5:c.317G>T	ENSP00000403035.1:p.Gly106Val
ENST00000455946.5:c.317G>T	ENSP00000416339.1:p.Gly106Val
ENST00000474944.5:n.337G>T
ENST00000475305.1:n.326G>T
ENST00000498673.5:c.-164G>T	ENSP00000430232.1:n.-164G>T
ENST00000518319.5:c.-203G>T	ENSP00000430289.1:n.-203G>T
ENST00000521065.1:c.223G>T
ENST00000521222.5:c.313G>T	ENSP00000429925.1:p.Val105Leu
ENST00000521517.5:c.309G>T
NM_001142301.1:c.-61G>T , LRG_688t2:c.-61G>T	NP_001135773.1:n.-61G>T
NM_153704.5:c.317G>T , LRG_688t1:c.317G>T	NP_714915.3:p.Gly106Val
NR_024522.1:n.388G>T
XM_006716686.2:c.14G>T	XP_006716749.1:p.Gly5Val
XM_011517363.1:c.317G>T	XP_011515665.1:p.Gly106Val
XR_428387.1:n.375G>T
XR_928360.1:n.375G>T
XR_928361.1:n.375G>T
XR_928362.1:n.375G>T
XM_006716686.4:c.14G>T	XP_006716749.1:p.Gly5Val
XM_011517363.3:c.317G>T	XP_011515665.1:p.Gly106Val
XM_024447326.1:c.-93G>T	XP_024303094.1:n.-93G>T
XR_001745619.2:n.358G>T
XR_428387.2:n.358G>T
XR_928360.3:n.358G>T
XR_928362.3:n.358G>T
NM_153704.6:c.317G>T MANE Select	NP_714915.3:p.Gly106Val
NR_024522.2:n.338G>T