Canonical Allele Identifier: CA1803221204
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780614T= , CM000670.2:g.93780614T= GRCh38
NC_000008.10:g.94792842T= , CM000670.1:g.94792842T= GRCh37
NC_000008.9:g.94862018T= NCBI36
NG_009190.1:g.30771T= , LRG_688:g.30771T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.736T= ENSP00000314488.4:p.Cys246=
ENST00000409623.8:c.736T= ENSP00000386966.4:p.Cys246=
ENST00000452276.6:c.736T= ENSP00000388671.2:p.Cys246=
ENST00000453906.6:c.407-5609T= ENSP00000403035.2:n.407-5609T=
ENST00000520680.2:c.736T= ENSP00000428785.2:p.Cys246=
ENST00000521065.2:c.*453T= ENSP00000427947.2:n.*453T=
ENST00000521517.6:c.736T= ENSP00000430740.2:p.Cys246=
ENST00000681998.1:c.666T= ENSP00000506773.1:n.666T=
ENST00000682036.1:c.407-5609T= ENSP00000508390.1:n.407-5609T=
ENST00000682577.1:c.666T= ENSP00000506963.1:n.666T=
ENST00000682624.1:c.*310T= ENSP00000508343.1:n.*310T=
ENST00000682700.1:c.736T= ENSP00000507627.1:p.Cys246=
ENST00000682744.1:n.274T=
ENST00000682804.1:n.559T=
ENST00000682837.1:c.491T= ENSP00000507920.1:p.Leu164=
ENST00000682935.1:n.2296T=
ENST00000682984.1:c.397T= ENSP00000507209.1:p.Cys133=
ENST00000683078.1:c.491T= ENSP00000506796.1:p.Leu164=
ENST00000683223.1:c.577T= ENSP00000507685.1:n.577T=
ENST00000683238.1:n.2117T=
ENST00000683249.1:n.2317T=
ENST00000683336.1:c.666T= ENSP00000507695.1:n.666T=
ENST00000683362.1:c.397T= ENSP00000506985.1:p.Cys133=
ENST00000683850.1:n.659T=
ENST00000683919.1:c.666T= ENSP00000507617.1:n.666T=
ENST00000683953.1:c.647T= ENSP00000508375.1:n.647T=
ENST00000684023.1:c.870T= ENSP00000507461.1:n.870T=
ENST00000684064.1:c.427T= ENSP00000508192.1:p.Cys143=
ENST00000684089.1:n.2286T=
ENST00000684149.1:c.*72T= ENSP00000507943.1:n.*72T=
ENST00000684416.1:n.695T=
ENST00000684540.1:c.666T= ENSP00000507987.1:n.666T=
ENST00000453321.8:c.736T= MANE Select ENSP00000389998.3:p.Cys246=
ENST00000323130.7:c.706T= ENSP00000314488.3:p.Cys236=
ENST00000409623.7:c.493T= ENSP00000386966.3:p.Cys165=
ENST00000425545.2:n.183T=
ENST00000452276.5:c.427T= ENSP00000388671.1:p.Cys143=
ENST00000453321.7:c.736T= ENSP00000389998.3:p.Cys246=
ENST00000453906.5:c.407-5609T= ENSP00000403035.1:n.407-5609T=
ENST00000474944.5:n.427-5609T=
ENST00000496213.5:n.201T=
NM_001142301.1:c.493T= , LRG_688t2:c.493T= NP_001135773.1:p.Cys165=
NM_153704.5:c.736T= , LRG_688t1:c.736T= NP_714915.3:p.Cys246=
NR_024522.1:n.807T=
XM_006716686.2:c.433T= XP_006716749.1:p.Cys145=
XM_006716687.2:c.136T= XP_006716750.1:p.Cys46=
XM_011517363.1:c.407-5609T= XP_011515665.1:n.407-5609T=
XR_428387.1:n.794T=
XR_928360.1:n.794T=
XR_928361.1:n.794T=
XR_928362.1:n.794T=
XM_006716686.4:c.433T= XP_006716749.1:p.Cys145=
XM_011517363.3:c.407-5609T= XP_011515665.1:n.407-5609T=
XM_024447326.1:c.82T= XP_024303094.1:p.Cys28=
XR_001745619.2:n.777T=
XR_428387.2:n.777T=
XR_928360.3:n.777T=
XR_928362.3:n.777T=
NM_153704.6:c.736T= MANE Select NP_714915.3:p.Cys246=
NR_024522.2:n.757T=