Canonical Allele Identifier: CA1803228215
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786338A= , CM000670.2:g.93786338A= GRCh38
NC_000008.10:g.94798566A= , CM000670.1:g.94798566A= GRCh37
NC_000008.9:g.94867742A= NCBI36
NG_009190.1:g.36495A= , LRG_688:g.36495A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1404A= ENSP00000314488.4:p.Ile468=
ENST00000409623.8:c.1359A= ENSP00000386966.4:p.Ile453=
ENST00000452276.6:c.1404A= ENSP00000388671.2:p.Ile468=
ENST00000453906.6:c.522A= ENSP00000403035.2:p.Ile174=
ENST00000520680.2:c.1404A= ENSP00000428785.2:p.Ile468=
ENST00000521517.6:c.1404A= ENSP00000430740.2:p.Ile468=
ENST00000681998.1:c.1225A= ENSP00000506773.1:n.1225A=
ENST00000682036.1:c.522A= ENSP00000508390.1:p.Ile174=
ENST00000682577.1:c.1177A= ENSP00000506963.1:n.1177A=
ENST00000682624.1:c.*978A= ENSP00000508343.1:n.*978A=
ENST00000682700.1:c.1404A= ENSP00000507627.1:p.Ile468=
ENST00000682744.1:n.942A=
ENST00000682804.1:n.1227A=
ENST00000682837.1:c.893A= ENSP00000507920.1:n.893A=
ENST00000682935.1:n.3454A=
ENST00000682984.1:c.1065A= ENSP00000507209.1:p.Ile355=
ENST00000683078.1:c.1159A= ENSP00000506796.1:n.1159A=
ENST00000683223.1:c.1136A= ENSP00000507685.1:n.1136A=
ENST00000683238.1:n.2628A=
ENST00000683249.1:n.3001A=
ENST00000683336.1:c.1225A= ENSP00000507695.1:n.1225A=
ENST00000683362.1:c.1065A= ENSP00000506985.1:p.Ile355=
ENST00000683850.1:n.1327A=
ENST00000683919.1:c.1334A= ENSP00000507617.1:n.1334A=
ENST00000683953.1:c.1315A= ENSP00000508375.1:n.1315A=
ENST00000684023.1:c.1381A= ENSP00000507461.1:n.1381A=
ENST00000684064.1:c.1095A= ENSP00000508192.1:p.Ile365=
ENST00000684089.1:n.2954A=
ENST00000684149.1:c.*583A= ENSP00000507943.1:n.*583A=
ENST00000684416.1:n.1363A=
ENST00000684540.1:c.1334A= ENSP00000507987.1:n.1334A=
ENST00000453321.8:c.1404A= MANE Select ENSP00000389998.3:p.Ile468=
ENST00000323130.7:c.1374A= ENSP00000314488.3:p.Ile458=
ENST00000409623.7:c.1161A= ENSP00000386966.3:p.Ile387=
ENST00000452276.5:c.1095A= ENSP00000388671.1:p.Ile365=
ENST00000453321.7:c.1404A= ENSP00000389998.3:p.Ile468=
ENST00000453906.5:c.522A= ENSP00000403035.1:p.Ile174=
ENST00000474944.5:n.542A=
ENST00000520680.1:c.226A=
NM_001142301.1:c.1161A= , LRG_688t2:c.1161A= NP_001135773.1:p.Ile387=
NM_153704.5:c.1404A= , LRG_688t1:c.1404A= NP_714915.3:p.Ile468=
NR_024522.1:n.1475A=
XM_006716686.2:c.1101A= XP_006716749.1:p.Ile367=
XM_006716687.2:c.804A= XP_006716750.1:p.Ile268=
XM_011517363.1:c.522A= XP_011515665.1:p.Ile174=
XR_428387.1:n.1462A=
XR_928360.1:n.1462A=
XR_928361.1:n.1462A=
XR_928362.1:n.1462A=
XM_006716686.4:c.1101A= XP_006716749.1:p.Ile367=
XM_011517363.3:c.522A= XP_011515665.1:p.Ile174=
XM_024447326.1:c.750A= XP_024303094.1:p.Ile250=
XR_001745619.2:n.1445A=
XR_428387.2:n.1445A=
XR_928360.3:n.1445A=
XR_928362.3:n.1445A=
NM_153704.6:c.1404A= MANE Select NP_714915.3:p.Ile468=
NR_024522.2:n.1425A=