Canonical Allele Identifier: CA371685746
Gene: TMEM67 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93758490T>A , CM000670.2:g.93758490T>A GRCh38
NC_000008.10:g.94770718T>A , CM000670.1:g.94770718T>A GRCh37
NC_000008.9:g.94839894T>A NCBI36
NG_009190.1:g.8647T>A , LRG_688:g.8647T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.320T>A ENSP00000314488.4:p.Val107Asp
ENST00000409623.8:c.320T>A ENSP00000386966.4:p.Val107Asp
ENST00000452276.6:c.320T>A ENSP00000388671.2:p.Val107Asp
ENST00000453906.6:c.320T>A ENSP00000403035.2:p.Val107Asp
ENST00000520680.2:c.320T>A ENSP00000428785.2:p.Val107Asp
ENST00000521065.2:c.320T>A ENSP00000427947.2:p.Val107Asp
ENST00000521517.6:c.320T>A ENSP00000430740.2:p.Val107Asp
ENST00000681998.1:c.320T>A ENSP00000506773.1:p.Val107Asp
ENST00000682036.1:c.320T>A ENSP00000508390.1:p.Val107Asp
ENST00000682577.1:c.320T>A ENSP00000506963.1:p.Val107Asp
ENST00000682624.1:c.231T>A ENSP00000508343.1:p.Cys77Ter
ENST00000682700.1:c.320T>A ENSP00000507627.1:p.Val107Asp
ENST00000682804.1:n.213T>A
ENST00000682837.1:c.320T>A ENSP00000507920.1:p.Val107Asp
ENST00000682935.1:n.320T>A
ENST00000682984.1:c.312+2624T>A ENSP00000507209.1:n.312+2624T>A
ENST00000683078.1:c.320T>A ENSP00000506796.1:p.Val107Asp
ENST00000683223.1:c.231T>A ENSP00000507685.1:p.Cys77Ter
ENST00000683238.1:n.141T>A
ENST00000683249.1:n.341T>A
ENST00000683336.1:c.320T>A ENSP00000507695.1:p.Val107Asp
ENST00000683362.1:c.312+2624T>A ENSP00000506985.1:n.312+2624T>A
ENST00000683850.1:n.243T>A
ENST00000683919.1:c.320T>A ENSP00000507617.1:p.Val107Asp
ENST00000683953.1:c.231T>A ENSP00000508375.1:p.Cys77Ter
ENST00000684023.1:c.320T>A ENSP00000507461.1:p.Val107Asp
ENST00000684064.1:c.11T>A ENSP00000508192.1:p.Val4Asp
ENST00000684089.1:n.310T>A
ENST00000684149.1:c.320T>A ENSP00000507943.1:p.Val107Asp
ENST00000684416.1:n.145T>A
ENST00000684540.1:c.320T>A ENSP00000507987.1:p.Val107Asp
ENST00000684733.1:n.255T>A
ENST00000453321.8:c.320T>A MANE Select ENSP00000389998.3:p.Val107Asp
ENST00000323130.7:c.290T>A ENSP00000314488.3:p.Val97Asp
ENST00000409623.7:c.-58T>A ENSP00000386966.3:n.-58T>A
ENST00000452276.5:c.11T>A ENSP00000388671.1:p.Val4Asp
ENST00000453321.7:c.320T>A ENSP00000389998.3:p.Val107Asp
ENST00000453906.5:c.320T>A ENSP00000403035.1:p.Val107Asp
ENST00000455946.5:c.320T>A ENSP00000416339.1:p.Val107Asp
ENST00000474944.5:n.340T>A
ENST00000475305.1:n.329T>A
ENST00000498673.5:c.-161T>A ENSP00000430232.1:n.-161T>A
ENST00000518319.5:c.-200T>A ENSP00000430289.1:n.-200T>A
ENST00000521065.1:c.226T>A
ENST00000521222.5:c.316T>A ENSP00000429925.1:p.Leu106Ile
ENST00000521517.5:c.312T>A
NM_001142301.1:c.-58T>A , LRG_688t2:c.-58T>A NP_001135773.1:n.-58T>A
NM_153704.5:c.320T>A , LRG_688t1:c.320T>A NP_714915.3:p.Val107Asp
NR_024522.1:n.391T>A
XM_006716686.2:c.17T>A XP_006716749.1:p.Val6Asp
XM_011517363.1:c.320T>A XP_011515665.1:p.Val107Asp
XR_428387.1:n.378T>A
XR_928360.1:n.378T>A
XR_928361.1:n.378T>A
XR_928362.1:n.378T>A
XM_006716686.4:c.17T>A XP_006716749.1:p.Val6Asp
XM_011517363.3:c.320T>A XP_011515665.1:p.Val107Asp
XM_024447326.1:c.-90T>A XP_024303094.1:n.-90T>A
XR_001745619.2:n.361T>A
XR_428387.2:n.361T>A
XR_928360.3:n.361T>A
XR_928362.3:n.361T>A
NM_153704.6:c.320T>A MANE Select NP_714915.3:p.Val107Asp
NR_024522.2:n.341T>A