Canonical Allele Identifier: CA1803227980
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786255C= , CM000670.2:g.93786255C= GRCh38
NC_000008.10:g.94798483C= , CM000670.1:g.94798483C= GRCh37
NC_000008.9:g.94867659C= NCBI36
NG_009190.1:g.36412C= , LRG_688:g.36412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1321C= ENSP00000314488.4:p.Arg441=
ENST00000409623.8:c.1289-13C= ENSP00000386966.4:n.1289-13C=
ENST00000452276.6:c.1321C= ENSP00000388671.2:p.Arg441=
ENST00000453906.6:c.439C= ENSP00000403035.2:p.Arg147=
ENST00000520680.2:c.1321C= ENSP00000428785.2:p.Arg441=
ENST00000521517.6:c.1321C= ENSP00000430740.2:p.Arg441=
ENST00000681998.1:c.1142C= ENSP00000506773.1:n.1142C=
ENST00000682036.1:c.439C= ENSP00000508390.1:p.Arg147=
ENST00000682577.1:c.1094C= ENSP00000506963.1:n.1094C=
ENST00000682624.1:c.*895C= ENSP00000508343.1:n.*895C=
ENST00000682700.1:c.1321C= ENSP00000507627.1:p.Arg441=
ENST00000682744.1:n.859C=
ENST00000682804.1:n.1144C=
ENST00000682837.1:c.810C= ENSP00000507920.1:n.810C=
ENST00000682935.1:n.3371C=
ENST00000682984.1:c.982C= ENSP00000507209.1:p.Arg328=
ENST00000683078.1:c.1076C= ENSP00000506796.1:n.1076C=
ENST00000683223.1:c.1053C= ENSP00000507685.1:n.1053C=
ENST00000683238.1:n.2545C=
ENST00000683249.1:n.2918C=
ENST00000683336.1:c.1142C= ENSP00000507695.1:n.1142C=
ENST00000683362.1:c.982C= ENSP00000506985.1:p.Arg328=
ENST00000683850.1:n.1244C=
ENST00000683919.1:c.1251C= ENSP00000507617.1:n.1251C=
ENST00000683953.1:c.1232C= ENSP00000508375.1:n.1232C=
ENST00000684023.1:c.1298C= ENSP00000507461.1:n.1298C=
ENST00000684064.1:c.1012C= ENSP00000508192.1:p.Arg338=
ENST00000684089.1:n.2871C=
ENST00000684149.1:c.*500C= ENSP00000507943.1:n.*500C=
ENST00000684416.1:n.1280C=
ENST00000684540.1:c.1251C= ENSP00000507987.1:n.1251C=
ENST00000453321.8:c.1321C= MANE Select ENSP00000389998.3:p.Arg441=
ENST00000323130.7:c.1291C= ENSP00000314488.3:p.Arg431=
ENST00000409623.7:c.1078C= ENSP00000386966.3:p.Arg360=
ENST00000452276.5:c.1012C= ENSP00000388671.1:p.Arg338=
ENST00000453321.7:c.1321C= ENSP00000389998.3:p.Arg441=
ENST00000453906.5:c.439C= ENSP00000403035.1:p.Arg147=
ENST00000474944.5:n.459C=
ENST00000520680.1:c.143C=
NM_001142301.1:c.1078C= , LRG_688t2:c.1078C= NP_001135773.1:p.Arg360=
NM_153704.5:c.1321C= , LRG_688t1:c.1321C= NP_714915.3:p.Arg441=
NR_024522.1:n.1392C=
XM_006716686.2:c.1018C= XP_006716749.1:p.Arg340=
XM_006716687.2:c.721C= XP_006716750.1:p.Arg241=
XM_011517363.1:c.439C= XP_011515665.1:p.Arg147=
XR_428387.1:n.1379C=
XR_928360.1:n.1379C=
XR_928361.1:n.1379C=
XR_928362.1:n.1379C=
XM_006716686.4:c.1018C= XP_006716749.1:p.Arg340=
XM_011517363.3:c.439C= XP_011515665.1:p.Arg147=
XM_024447326.1:c.667C= XP_024303094.1:p.Arg223=
XR_001745619.2:n.1362C=
XR_428387.2:n.1362C=
XR_928360.3:n.1362C=
XR_928362.3:n.1362C=
NM_153704.6:c.1321C= MANE Select NP_714915.3:p.Arg441=
NR_024522.2:n.1342C=