Canonical Allele Identifier: CA1803221877
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780930T= , CM000670.2:g.93780930T= GRCh38
NC_000008.10:g.94793158T= , CM000670.1:g.94793158T= GRCh37
NC_000008.9:g.94862334T= NCBI36
NG_009190.1:g.31087T= , LRG_688:g.31087T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.926T= ENSP00000314488.4:p.Val309=
ENST00000409623.8:c.926T= ENSP00000386966.4:p.Val309=
ENST00000452276.6:c.926T= ENSP00000388671.2:p.Val309=
ENST00000453906.6:c.407-5293T= ENSP00000403035.2:n.407-5293T=
ENST00000520680.2:c.926T= ENSP00000428785.2:p.Val309=
ENST00000521065.2:c.*643T= ENSP00000427947.2:n.*643T=
ENST00000521517.6:c.926T= ENSP00000430740.2:p.Val309=
ENST00000681998.1:c.799+183T= ENSP00000506773.1:n.799+183T=
ENST00000682036.1:c.407-5293T= ENSP00000508390.1:n.407-5293T=
ENST00000682577.1:c.856T= ENSP00000506963.1:n.856T=
ENST00000682624.1:c.*500T= ENSP00000508343.1:n.*500T=
ENST00000682700.1:c.926T= ENSP00000507627.1:p.Val309=
ENST00000682744.1:n.464T=
ENST00000682804.1:n.749T=
ENST00000682837.1:c.624+183T= ENSP00000507920.1:n.624+183T=
ENST00000682935.1:n.2486T=
ENST00000682984.1:c.587T= ENSP00000507209.1:p.Val196=
ENST00000683078.1:c.681T= ENSP00000506796.1:n.681T=
ENST00000683223.1:c.710+183T= ENSP00000507685.1:n.710+183T=
ENST00000683238.1:n.2307T=
ENST00000683249.1:n.2523T=
ENST00000683336.1:c.799+183T= ENSP00000507695.1:n.799+183T=
ENST00000683362.1:c.587T= ENSP00000506985.1:p.Val196=
ENST00000683850.1:n.849T=
ENST00000683919.1:c.856T= ENSP00000507617.1:n.856T=
ENST00000683953.1:c.837T= ENSP00000508375.1:n.837T=
ENST00000684023.1:c.1060T= ENSP00000507461.1:n.1060T=
ENST00000684064.1:c.617T= ENSP00000508192.1:p.Val206=
ENST00000684089.1:n.2476T=
ENST00000684149.1:c.*262T= ENSP00000507943.1:n.*262T=
ENST00000684416.1:n.885T=
ENST00000684540.1:c.856T= ENSP00000507987.1:n.856T=
ENST00000453321.8:c.926T= MANE Select ENSP00000389998.3:p.Val309=
ENST00000323130.7:c.896T= ENSP00000314488.3:p.Val299=
ENST00000409623.7:c.683T= ENSP00000386966.3:p.Val228=
ENST00000425545.2:n.373T=
ENST00000452276.5:c.617T= ENSP00000388671.1:p.Val206=
ENST00000453321.7:c.926T= ENSP00000389998.3:p.Val309=
ENST00000453906.5:c.407-5293T= ENSP00000403035.1:n.407-5293T=
ENST00000474944.5:n.427-5293T=
ENST00000496213.5:n.391T=
NM_001142301.1:c.683T= , LRG_688t2:c.683T= NP_001135773.1:p.Val228=
NM_153704.5:c.926T= , LRG_688t1:c.926T= NP_714915.3:p.Val309=
NR_024522.1:n.997T=
XM_006716686.2:c.623T= XP_006716749.1:p.Val208=
XM_006716687.2:c.326T= XP_006716750.1:p.Val109=
XM_011517363.1:c.407-5293T= XP_011515665.1:n.407-5293T=
XR_428387.1:n.984T=
XR_928360.1:n.984T=
XR_928361.1:n.984T=
XR_928362.1:n.984T=
XM_006716686.4:c.623T= XP_006716749.1:p.Val208=
XM_011517363.3:c.407-5293T= XP_011515665.1:n.407-5293T=
XM_024447326.1:c.272T= XP_024303094.1:p.Val91=
XR_001745619.2:n.967T=
XR_428387.2:n.967T=
XR_928360.3:n.967T=
XR_928362.3:n.967T=
NM_153704.6:c.926T= MANE Select NP_714915.3:p.Val309=
NR_024522.2:n.947T=