Canonical Allele Identifier: CA1803221292
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780643G= , CM000670.2:g.93780643G= GRCh38
NC_000008.10:g.94792871G= , CM000670.1:g.94792871G= GRCh37
NC_000008.9:g.94862047G= NCBI36
NG_009190.1:g.30800G= , LRG_688:g.30800G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.765G= ENSP00000314488.4:p.Met255=
ENST00000409623.8:c.765G= ENSP00000386966.4:p.Met255=
ENST00000452276.6:c.765G= ENSP00000388671.2:p.Met255=
ENST00000453906.6:c.407-5580G= ENSP00000403035.2:n.407-5580G=
ENST00000520680.2:c.765G= ENSP00000428785.2:p.Met255=
ENST00000521065.2:c.*482G= ENSP00000427947.2:n.*482G=
ENST00000521517.6:c.765G= ENSP00000430740.2:p.Met255=
ENST00000681998.1:c.695G= ENSP00000506773.1:n.695G=
ENST00000682036.1:c.407-5580G= ENSP00000508390.1:n.407-5580G=
ENST00000682577.1:c.695G= ENSP00000506963.1:n.695G=
ENST00000682624.1:c.*339G= ENSP00000508343.1:n.*339G=
ENST00000682700.1:c.765G= ENSP00000507627.1:p.Met255=
ENST00000682744.1:n.303G=
ENST00000682804.1:n.588G=
ENST00000682837.1:c.520G= ENSP00000507920.1:p.Glu174=
ENST00000682935.1:n.2325G=
ENST00000682984.1:c.426G= ENSP00000507209.1:p.Met142=
ENST00000683078.1:c.520G= ENSP00000506796.1:p.Glu174=
ENST00000683223.1:c.606G= ENSP00000507685.1:n.606G=
ENST00000683238.1:n.2146G=
ENST00000683249.1:n.2346G=
ENST00000683336.1:c.695G= ENSP00000507695.1:n.695G=
ENST00000683362.1:c.426G= ENSP00000506985.1:p.Met142=
ENST00000683850.1:n.688G=
ENST00000683919.1:c.695G= ENSP00000507617.1:n.695G=
ENST00000683953.1:c.676G= ENSP00000508375.1:n.676G=
ENST00000684023.1:c.899G= ENSP00000507461.1:n.899G=
ENST00000684064.1:c.456G= ENSP00000508192.1:p.Met152=
ENST00000684089.1:n.2315G=
ENST00000684149.1:c.*101G= ENSP00000507943.1:n.*101G=
ENST00000684416.1:n.724G=
ENST00000684540.1:c.695G= ENSP00000507987.1:n.695G=
ENST00000453321.8:c.765G= MANE Select ENSP00000389998.3:p.Met255=
ENST00000323130.7:c.735G= ENSP00000314488.3:p.Met245=
ENST00000409623.7:c.522G= ENSP00000386966.3:p.Met174=
ENST00000425545.2:n.212G=
ENST00000452276.5:c.456G= ENSP00000388671.1:p.Met152=
ENST00000453321.7:c.765G= ENSP00000389998.3:p.Met255=
ENST00000453906.5:c.407-5580G= ENSP00000403035.1:n.407-5580G=
ENST00000474944.5:n.427-5580G=
ENST00000496213.5:n.230G=
NM_001142301.1:c.522G= , LRG_688t2:c.522G= NP_001135773.1:p.Met174=
NM_153704.5:c.765G= , LRG_688t1:c.765G= NP_714915.3:p.Met255=
NR_024522.1:n.836G=
XM_006716686.2:c.462G= XP_006716749.1:p.Met154=
XM_006716687.2:c.165G= XP_006716750.1:p.Met55=
XM_011517363.1:c.407-5580G= XP_011515665.1:n.407-5580G=
XR_428387.1:n.823G=
XR_928360.1:n.823G=
XR_928361.1:n.823G=
XR_928362.1:n.823G=
XM_006716686.4:c.462G= XP_006716749.1:p.Met154=
XM_011517363.3:c.407-5580G= XP_011515665.1:n.407-5580G=
XM_024447326.1:c.111G= XP_024303094.1:p.Met37=
XR_001745619.2:n.806G=
XR_428387.2:n.806G=
XR_928360.3:n.806G=
XR_928362.3:n.806G=
NM_153704.6:c.765G= MANE Select NP_714915.3:p.Met255=
NR_024522.2:n.786G=