Canonical Allele Identifier: CA371689860

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94798565T>G (hg19) ; chr8:g.93786337T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93786337T>G , CM000670.2:g.93786337T>G	GRCh38
NC_000008.10:g.94798565T>G , CM000670.1:g.94798565T>G	GRCh37
NC_000008.9:g.94867741T>G	NCBI36
NG_009190.1:g.36494T>G , LRG_688:g.36494T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.1403T>G	ENSP00000314488.4:p.Ile468Arg
ENST00000409623.8:c.1358T>G	ENSP00000386966.4:p.Ile453Arg
ENST00000452276.6:c.1403T>G	ENSP00000388671.2:p.Ile468Arg
ENST00000453906.6:c.521T>G	ENSP00000403035.2:p.Ile174Arg
ENST00000520680.2:c.1403T>G	ENSP00000428785.2:p.Ile468Arg
ENST00000521517.6:c.1403T>G	ENSP00000430740.2:p.Ile468Arg
ENST00000681998.1:c.1224T>G	ENSP00000506773.1:n.1224T>G
ENST00000682036.1:c.521T>G	ENSP00000508390.1:p.Ile174Arg
ENST00000682577.1:c.1176T>G	ENSP00000506963.1:n.1176T>G
ENST00000682624.1:c.*977T>G	ENSP00000508343.1:n.*977T>G
ENST00000682700.1:c.1403T>G	ENSP00000507627.1:p.Ile468Arg
ENST00000682744.1:n.941T>G
ENST00000682804.1:n.1226T>G
ENST00000682837.1:c.892T>G	ENSP00000507920.1:n.892T>G
ENST00000682935.1:n.3453T>G
ENST00000682984.1:c.1064T>G	ENSP00000507209.1:p.Ile355Arg
ENST00000683078.1:c.1158T>G	ENSP00000506796.1:n.1158T>G
ENST00000683223.1:c.1135T>G	ENSP00000507685.1:n.1135T>G
ENST00000683238.1:n.2627T>G
ENST00000683249.1:n.3000T>G
ENST00000683336.1:c.1224T>G	ENSP00000507695.1:n.1224T>G
ENST00000683362.1:c.1064T>G	ENSP00000506985.1:p.Ile355Arg
ENST00000683850.1:n.1326T>G
ENST00000683919.1:c.1333T>G	ENSP00000507617.1:n.1333T>G
ENST00000683953.1:c.1314T>G	ENSP00000508375.1:n.1314T>G
ENST00000684023.1:c.1380T>G	ENSP00000507461.1:n.1380T>G
ENST00000684064.1:c.1094T>G	ENSP00000508192.1:p.Ile365Arg
ENST00000684089.1:n.2953T>G
ENST00000684149.1:c.*582T>G	ENSP00000507943.1:n.*582T>G
ENST00000684416.1:n.1362T>G
ENST00000684540.1:c.1333T>G	ENSP00000507987.1:n.1333T>G
ENST00000453321.8:c.1403T>G MANE Select	ENSP00000389998.3:p.Ile468Arg
ENST00000323130.7:c.1373T>G	ENSP00000314488.3:p.Ile458Arg
ENST00000409623.7:c.1160T>G	ENSP00000386966.3:p.Ile387Arg
ENST00000452276.5:c.1094T>G	ENSP00000388671.1:p.Ile365Arg
ENST00000453321.7:c.1403T>G	ENSP00000389998.3:p.Ile468Arg
ENST00000453906.5:c.521T>G	ENSP00000403035.1:p.Ile174Arg
ENST00000474944.5:n.541T>G
ENST00000520680.1:c.225T>G
NM_001142301.1:c.1160T>G , LRG_688t2:c.1160T>G	NP_001135773.1:p.Ile387Arg
NM_153704.5:c.1403T>G , LRG_688t1:c.1403T>G	NP_714915.3:p.Ile468Arg
NR_024522.1:n.1474T>G
XM_006716686.2:c.1100T>G	XP_006716749.1:p.Ile367Arg
XM_006716687.2:c.803T>G	XP_006716750.1:p.Ile268Arg
XM_011517363.1:c.521T>G	XP_011515665.1:p.Ile174Arg
XR_428387.1:n.1461T>G
XR_928360.1:n.1461T>G
XR_928361.1:n.1461T>G
XR_928362.1:n.1461T>G
XM_006716686.4:c.1100T>G	XP_006716749.1:p.Ile367Arg
XM_011517363.3:c.521T>G	XP_011515665.1:p.Ile174Arg
XM_024447326.1:c.749T>G	XP_024303094.1:p.Ile250Arg
XR_001745619.2:n.1444T>G
XR_428387.2:n.1444T>G
XR_928360.3:n.1444T>G
XR_928362.3:n.1444T>G
NM_153704.6:c.1403T>G MANE Select	NP_714915.3:p.Ile468Arg
NR_024522.2:n.1424T>G