Canonical Allele Identifier: CA1803228003
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786270G= , CM000670.2:g.93786270G= GRCh38
NC_000008.10:g.94798498G= , CM000670.1:g.94798498G= GRCh37
NC_000008.9:g.94867674G= NCBI36
NG_009190.1:g.36427G= , LRG_688:g.36427G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1336G= ENSP00000314488.4:p.Asp446=
ENST00000409623.8:c.1291G= ENSP00000386966.4:p.Asp431=
ENST00000452276.6:c.1336G= ENSP00000388671.2:p.Asp446=
ENST00000453906.6:c.454G= ENSP00000403035.2:p.Asp152=
ENST00000520680.2:c.1336G= ENSP00000428785.2:p.Asp446=
ENST00000521517.6:c.1336G= ENSP00000430740.2:p.Asp446=
ENST00000681998.1:c.1157G= ENSP00000506773.1:n.1157G=
ENST00000682036.1:c.454G= ENSP00000508390.1:p.Asp152=
ENST00000682577.1:c.1109G= ENSP00000506963.1:n.1109G=
ENST00000682624.1:c.*910G= ENSP00000508343.1:n.*910G=
ENST00000682700.1:c.1336G= ENSP00000507627.1:p.Asp446=
ENST00000682744.1:n.874G=
ENST00000682804.1:n.1159G=
ENST00000682837.1:c.825G= ENSP00000507920.1:n.825G=
ENST00000682935.1:n.3386G=
ENST00000682984.1:c.997G= ENSP00000507209.1:p.Asp333=
ENST00000683078.1:c.1091G= ENSP00000506796.1:n.1091G=
ENST00000683223.1:c.1068G= ENSP00000507685.1:n.1068G=
ENST00000683238.1:n.2560G=
ENST00000683249.1:n.2933G=
ENST00000683336.1:c.1157G= ENSP00000507695.1:n.1157G=
ENST00000683362.1:c.997G= ENSP00000506985.1:p.Asp333=
ENST00000683850.1:n.1259G=
ENST00000683919.1:c.1266G= ENSP00000507617.1:n.1266G=
ENST00000683953.1:c.1247G= ENSP00000508375.1:n.1247G=
ENST00000684023.1:c.1313G= ENSP00000507461.1:n.1313G=
ENST00000684064.1:c.1027G= ENSP00000508192.1:p.Asp343=
ENST00000684089.1:n.2886G=
ENST00000684149.1:c.*515G= ENSP00000507943.1:n.*515G=
ENST00000684416.1:n.1295G=
ENST00000684540.1:c.1266G= ENSP00000507987.1:n.1266G=
ENST00000453321.8:c.1336G= MANE Select ENSP00000389998.3:p.Asp446=
ENST00000323130.7:c.1306G= ENSP00000314488.3:p.Asp436=
ENST00000409623.7:c.1093G= ENSP00000386966.3:p.Asp365=
ENST00000452276.5:c.1027G= ENSP00000388671.1:p.Asp343=
ENST00000453321.7:c.1336G= ENSP00000389998.3:p.Asp446=
ENST00000453906.5:c.454G= ENSP00000403035.1:p.Asp152=
ENST00000474944.5:n.474G=
ENST00000520680.1:c.158G=
NM_001142301.1:c.1093G= , LRG_688t2:c.1093G= NP_001135773.1:p.Asp365=
NM_153704.5:c.1336G= , LRG_688t1:c.1336G= NP_714915.3:p.Asp446=
NR_024522.1:n.1407G=
XM_006716686.2:c.1033G= XP_006716749.1:p.Asp345=
XM_006716687.2:c.736G= XP_006716750.1:p.Asp246=
XM_011517363.1:c.454G= XP_011515665.1:p.Asp152=
XR_428387.1:n.1394G=
XR_928360.1:n.1394G=
XR_928361.1:n.1394G=
XR_928362.1:n.1394G=
XM_006716686.4:c.1033G= XP_006716749.1:p.Asp345=
XM_011517363.3:c.454G= XP_011515665.1:p.Asp152=
XM_024447326.1:c.682G= XP_024303094.1:p.Asp228=
XR_001745619.2:n.1377G=
XR_428387.2:n.1377G=
XR_928360.3:n.1377G=
XR_928362.3:n.1377G=
NM_153704.6:c.1336G= MANE Select NP_714915.3:p.Asp446=
NR_024522.2:n.1357G=