Canonical Allele Identifier: CA1803228164
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786322G= , CM000670.2:g.93786322G= GRCh38
NC_000008.10:g.94798550G= , CM000670.1:g.94798550G= GRCh37
NC_000008.9:g.94867726G= NCBI36
NG_009190.1:g.36479G= , LRG_688:g.36479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1388G= ENSP00000314488.4:p.Arg463=
ENST00000409623.8:c.1343G= ENSP00000386966.4:p.Arg448=
ENST00000452276.6:c.1388G= ENSP00000388671.2:p.Arg463=
ENST00000453906.6:c.506G= ENSP00000403035.2:p.Arg169=
ENST00000520680.2:c.1388G= ENSP00000428785.2:p.Arg463=
ENST00000521517.6:c.1388G= ENSP00000430740.2:p.Arg463=
ENST00000681998.1:c.1209G= ENSP00000506773.1:n.1209G=
ENST00000682036.1:c.506G= ENSP00000508390.1:p.Arg169=
ENST00000682577.1:c.1161G= ENSP00000506963.1:n.1161G=
ENST00000682624.1:c.*962G= ENSP00000508343.1:n.*962G=
ENST00000682700.1:c.1388G= ENSP00000507627.1:p.Arg463=
ENST00000682744.1:n.926G=
ENST00000682804.1:n.1211G=
ENST00000682837.1:c.877G= ENSP00000507920.1:n.877G=
ENST00000682935.1:n.3438G=
ENST00000682984.1:c.1049G= ENSP00000507209.1:p.Arg350=
ENST00000683078.1:c.1143G= ENSP00000506796.1:n.1143G=
ENST00000683223.1:c.1120G= ENSP00000507685.1:n.1120G=
ENST00000683238.1:n.2612G=
ENST00000683249.1:n.2985G=
ENST00000683336.1:c.1209G= ENSP00000507695.1:n.1209G=
ENST00000683362.1:c.1049G= ENSP00000506985.1:p.Arg350=
ENST00000683850.1:n.1311G=
ENST00000683919.1:c.1318G= ENSP00000507617.1:n.1318G=
ENST00000683953.1:c.1299G= ENSP00000508375.1:n.1299G=
ENST00000684023.1:c.1365G= ENSP00000507461.1:n.1365G=
ENST00000684064.1:c.1079G= ENSP00000508192.1:p.Arg360=
ENST00000684089.1:n.2938G=
ENST00000684149.1:c.*567G= ENSP00000507943.1:n.*567G=
ENST00000684416.1:n.1347G=
ENST00000684540.1:c.1318G= ENSP00000507987.1:n.1318G=
ENST00000453321.8:c.1388G= MANE Select ENSP00000389998.3:p.Arg463=
ENST00000323130.7:c.1358G= ENSP00000314488.3:p.Arg453=
ENST00000409623.7:c.1145G= ENSP00000386966.3:p.Arg382=
ENST00000452276.5:c.1079G= ENSP00000388671.1:p.Arg360=
ENST00000453321.7:c.1388G= ENSP00000389998.3:p.Arg463=
ENST00000453906.5:c.506G= ENSP00000403035.1:p.Arg169=
ENST00000474944.5:n.526G=
ENST00000520680.1:c.210G=
NM_001142301.1:c.1145G= , LRG_688t2:c.1145G= NP_001135773.1:p.Arg382=
NM_153704.5:c.1388G= , LRG_688t1:c.1388G= NP_714915.3:p.Arg463=
NR_024522.1:n.1459G=
XM_006716686.2:c.1085G= XP_006716749.1:p.Arg362=
XM_006716687.2:c.788G= XP_006716750.1:p.Arg263=
XM_011517363.1:c.506G= XP_011515665.1:p.Arg169=
XR_428387.1:n.1446G=
XR_928360.1:n.1446G=
XR_928361.1:n.1446G=
XR_928362.1:n.1446G=
XM_006716686.4:c.1085G= XP_006716749.1:p.Arg362=
XM_011517363.3:c.506G= XP_011515665.1:p.Arg169=
XM_024447326.1:c.734G= XP_024303094.1:p.Arg245=
XR_001745619.2:n.1429G=
XR_428387.2:n.1429G=
XR_928360.3:n.1429G=
XR_928362.3:n.1429G=
NM_153704.6:c.1388G= MANE Select NP_714915.3:p.Arg463=
NR_024522.2:n.1409G=