Canonical Allele Identifier: CA1803228042
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786285C= , CM000670.2:g.93786285C= GRCh38
NC_000008.10:g.94798513C= , CM000670.1:g.94798513C= GRCh37
NC_000008.9:g.94867689C= NCBI36
NG_009190.1:g.36442C= , LRG_688:g.36442C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1351C= ENSP00000314488.4:p.Arg451=
ENST00000409623.8:c.1306C= ENSP00000386966.4:p.Arg436=
ENST00000452276.6:c.1351C= ENSP00000388671.2:p.Arg451=
ENST00000453906.6:c.469C= ENSP00000403035.2:p.Arg157=
ENST00000520680.2:c.1351C= ENSP00000428785.2:p.Arg451=
ENST00000521517.6:c.1351C= ENSP00000430740.2:p.Arg451=
ENST00000681998.1:c.1172C= ENSP00000506773.1:n.1172C=
ENST00000682036.1:c.469C= ENSP00000508390.1:p.Arg157=
ENST00000682577.1:c.1124C= ENSP00000506963.1:n.1124C=
ENST00000682624.1:c.*925C= ENSP00000508343.1:n.*925C=
ENST00000682700.1:c.1351C= ENSP00000507627.1:p.Arg451=
ENST00000682744.1:n.889C=
ENST00000682804.1:n.1174C=
ENST00000682837.1:c.840C= ENSP00000507920.1:n.840C=
ENST00000682935.1:n.3401C=
ENST00000682984.1:c.1012C= ENSP00000507209.1:p.Arg338=
ENST00000683078.1:c.1106C= ENSP00000506796.1:n.1106C=
ENST00000683223.1:c.1083C= ENSP00000507685.1:n.1083C=
ENST00000683238.1:n.2575C=
ENST00000683249.1:n.2948C=
ENST00000683336.1:c.1172C= ENSP00000507695.1:n.1172C=
ENST00000683362.1:c.1012C= ENSP00000506985.1:p.Arg338=
ENST00000683850.1:n.1274C=
ENST00000683919.1:c.1281C= ENSP00000507617.1:n.1281C=
ENST00000683953.1:c.1262C= ENSP00000508375.1:n.1262C=
ENST00000684023.1:c.1328C= ENSP00000507461.1:n.1328C=
ENST00000684064.1:c.1042C= ENSP00000508192.1:p.Arg348=
ENST00000684089.1:n.2901C=
ENST00000684149.1:c.*530C= ENSP00000507943.1:n.*530C=
ENST00000684416.1:n.1310C=
ENST00000684540.1:c.1281C= ENSP00000507987.1:n.1281C=
ENST00000453321.8:c.1351C= MANE Select ENSP00000389998.3:p.Arg451=
ENST00000323130.7:c.1321C= ENSP00000314488.3:p.Arg441=
ENST00000409623.7:c.1108C= ENSP00000386966.3:p.Arg370=
ENST00000452276.5:c.1042C= ENSP00000388671.1:p.Arg348=
ENST00000453321.7:c.1351C= ENSP00000389998.3:p.Arg451=
ENST00000453906.5:c.469C= ENSP00000403035.1:p.Arg157=
ENST00000474944.5:n.489C=
ENST00000520680.1:c.173C=
NM_001142301.1:c.1108C= , LRG_688t2:c.1108C= NP_001135773.1:p.Arg370=
NM_153704.5:c.1351C= , LRG_688t1:c.1351C= NP_714915.3:p.Arg451=
NR_024522.1:n.1422C=
XM_006716686.2:c.1048C= XP_006716749.1:p.Arg350=
XM_006716687.2:c.751C= XP_006716750.1:p.Arg251=
XM_011517363.1:c.469C= XP_011515665.1:p.Arg157=
XR_428387.1:n.1409C=
XR_928360.1:n.1409C=
XR_928361.1:n.1409C=
XR_928362.1:n.1409C=
XM_006716686.4:c.1048C= XP_006716749.1:p.Arg350=
XM_011517363.3:c.469C= XP_011515665.1:p.Arg157=
XM_024447326.1:c.697C= XP_024303094.1:p.Arg233=
XR_001745619.2:n.1392C=
XR_428387.2:n.1392C=
XR_928360.3:n.1392C=
XR_928362.3:n.1392C=
NM_153704.6:c.1351C= MANE Select NP_714915.3:p.Arg451=
NR_024522.2:n.1372C=