Canonical Allele Identifier: CA1803221812
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780891G= , CM000670.2:g.93780891G= GRCh38
NC_000008.10:g.94793119G= , CM000670.1:g.94793119G= GRCh37
NC_000008.9:g.94862295G= NCBI36
NG_009190.1:g.31048G= , LRG_688:g.31048G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.887G= ENSP00000314488.4:p.Trp296=
ENST00000409623.8:c.887G= ENSP00000386966.4:p.Trp296=
ENST00000452276.6:c.887G= ENSP00000388671.2:p.Trp296=
ENST00000453906.6:c.407-5332G= ENSP00000403035.2:n.407-5332G=
ENST00000520680.2:c.887G= ENSP00000428785.2:p.Trp296=
ENST00000521065.2:c.*604G= ENSP00000427947.2:n.*604G=
ENST00000521517.6:c.887G= ENSP00000430740.2:p.Trp296=
ENST00000681998.1:c.799+144G= ENSP00000506773.1:n.799+144G=
ENST00000682036.1:c.407-5332G= ENSP00000508390.1:n.407-5332G=
ENST00000682577.1:c.817G= ENSP00000506963.1:n.817G=
ENST00000682624.1:c.*461G= ENSP00000508343.1:n.*461G=
ENST00000682700.1:c.887G= ENSP00000507627.1:p.Trp296=
ENST00000682744.1:n.425G=
ENST00000682804.1:n.710G=
ENST00000682837.1:c.624+144G= ENSP00000507920.1:n.624+144G=
ENST00000682935.1:n.2447G=
ENST00000682984.1:c.548G= ENSP00000507209.1:p.Trp183=
ENST00000683078.1:c.642G= ENSP00000506796.1:n.642G=
ENST00000683223.1:c.710+144G= ENSP00000507685.1:n.710+144G=
ENST00000683238.1:n.2268G=
ENST00000683249.1:n.2484G=
ENST00000683336.1:c.799+144G= ENSP00000507695.1:n.799+144G=
ENST00000683362.1:c.548G= ENSP00000506985.1:p.Trp183=
ENST00000683850.1:n.810G=
ENST00000683919.1:c.817G= ENSP00000507617.1:n.817G=
ENST00000683953.1:c.798G= ENSP00000508375.1:n.798G=
ENST00000684023.1:c.1021G= ENSP00000507461.1:n.1021G=
ENST00000684064.1:c.578G= ENSP00000508192.1:p.Trp193=
ENST00000684089.1:n.2437G=
ENST00000684149.1:c.*223G= ENSP00000507943.1:n.*223G=
ENST00000684416.1:n.846G=
ENST00000684540.1:c.817G= ENSP00000507987.1:n.817G=
ENST00000453321.8:c.887G= MANE Select ENSP00000389998.3:p.Trp296=
ENST00000323130.7:c.857G= ENSP00000314488.3:p.Trp286=
ENST00000409623.7:c.644G= ENSP00000386966.3:p.Trp215=
ENST00000425545.2:n.334G=
ENST00000452276.5:c.578G= ENSP00000388671.1:p.Trp193=
ENST00000453321.7:c.887G= ENSP00000389998.3:p.Trp296=
ENST00000453906.5:c.407-5332G= ENSP00000403035.1:n.407-5332G=
ENST00000474944.5:n.427-5332G=
ENST00000496213.5:n.352G=
NM_001142301.1:c.644G= , LRG_688t2:c.644G= NP_001135773.1:p.Trp215=
NM_153704.5:c.887G= , LRG_688t1:c.887G= NP_714915.3:p.Trp296=
NR_024522.1:n.958G=
XM_006716686.2:c.584G= XP_006716749.1:p.Trp195=
XM_006716687.2:c.287G= XP_006716750.1:p.Trp96=
XM_011517363.1:c.407-5332G= XP_011515665.1:n.407-5332G=
XR_428387.1:n.945G=
XR_928360.1:n.945G=
XR_928361.1:n.945G=
XR_928362.1:n.945G=
XM_006716686.4:c.584G= XP_006716749.1:p.Trp195=
XM_011517363.3:c.407-5332G= XP_011515665.1:n.407-5332G=
XM_024447326.1:c.233G= XP_024303094.1:p.Trp78=
XR_001745619.2:n.928G=
XR_428387.2:n.928G=
XR_928360.3:n.928G=
XR_928362.3:n.928G=
NM_153704.6:c.887G= MANE Select NP_714915.3:p.Trp296=
NR_024522.2:n.908G=