Canonical Allele Identifier: CA1803221305
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780647A= , CM000670.2:g.93780647A= GRCh38
NC_000008.10:g.94792875A= , CM000670.1:g.94792875A= GRCh37
NC_000008.9:g.94862051A= NCBI36
NG_009190.1:g.30804A= , LRG_688:g.30804A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.769A= ENSP00000314488.4:p.Met257=
ENST00000409623.8:c.769A= ENSP00000386966.4:p.Met257=
ENST00000452276.6:c.769A= ENSP00000388671.2:p.Met257=
ENST00000453906.6:c.407-5576A= ENSP00000403035.2:n.407-5576A=
ENST00000520680.2:c.769A= ENSP00000428785.2:p.Met257=
ENST00000521065.2:c.*486A= ENSP00000427947.2:n.*486A=
ENST00000521517.6:c.769A= ENSP00000430740.2:p.Met257=
ENST00000681998.1:c.699A= ENSP00000506773.1:n.699A=
ENST00000682036.1:c.407-5576A= ENSP00000508390.1:n.407-5576A=
ENST00000682577.1:c.699A= ENSP00000506963.1:n.699A=
ENST00000682624.1:c.*343A= ENSP00000508343.1:n.*343A=
ENST00000682700.1:c.769A= ENSP00000507627.1:p.Met257=
ENST00000682744.1:n.307A=
ENST00000682804.1:n.592A=
ENST00000682837.1:c.524A= ENSP00000507920.1:p.His175=
ENST00000682935.1:n.2329A=
ENST00000682984.1:c.430A= ENSP00000507209.1:p.Met144=
ENST00000683078.1:c.524A= ENSP00000506796.1:p.His175=
ENST00000683223.1:c.610A= ENSP00000507685.1:n.610A=
ENST00000683238.1:n.2150A=
ENST00000683249.1:n.2350A=
ENST00000683336.1:c.699A= ENSP00000507695.1:n.699A=
ENST00000683362.1:c.430A= ENSP00000506985.1:p.Met144=
ENST00000683850.1:n.692A=
ENST00000683919.1:c.699A= ENSP00000507617.1:n.699A=
ENST00000683953.1:c.680A= ENSP00000508375.1:n.680A=
ENST00000684023.1:c.903A= ENSP00000507461.1:n.903A=
ENST00000684064.1:c.460A= ENSP00000508192.1:p.Met154=
ENST00000684089.1:n.2319A=
ENST00000684149.1:c.*105A= ENSP00000507943.1:n.*105A=
ENST00000684416.1:n.728A=
ENST00000684540.1:c.699A= ENSP00000507987.1:n.699A=
ENST00000453321.8:c.769A= MANE Select ENSP00000389998.3:p.Met257=
ENST00000323130.7:c.739A= ENSP00000314488.3:p.Met247=
ENST00000409623.7:c.526A= ENSP00000386966.3:p.Met176=
ENST00000425545.2:n.216A=
ENST00000452276.5:c.460A= ENSP00000388671.1:p.Met154=
ENST00000453321.7:c.769A= ENSP00000389998.3:p.Met257=
ENST00000453906.5:c.407-5576A= ENSP00000403035.1:n.407-5576A=
ENST00000474944.5:n.427-5576A=
ENST00000496213.5:n.234A=
NM_001142301.1:c.526A= , LRG_688t2:c.526A= NP_001135773.1:p.Met176=
NM_153704.5:c.769A= , LRG_688t1:c.769A= NP_714915.3:p.Met257=
NR_024522.1:n.840A=
XM_006716686.2:c.466A= XP_006716749.1:p.Met156=
XM_006716687.2:c.169A= XP_006716750.1:p.Met57=
XM_011517363.1:c.407-5576A= XP_011515665.1:n.407-5576A=
XR_428387.1:n.827A=
XR_928360.1:n.827A=
XR_928361.1:n.827A=
XR_928362.1:n.827A=
XM_006716686.4:c.466A= XP_006716749.1:p.Met156=
XM_011517363.3:c.407-5576A= XP_011515665.1:n.407-5576A=
XM_024447326.1:c.115A= XP_024303094.1:p.Met39=
XR_001745619.2:n.810A=
XR_428387.2:n.810A=
XR_928360.3:n.810A=
XR_928362.3:n.810A=
NM_153704.6:c.769A= MANE Select NP_714915.3:p.Met257=
NR_024522.2:n.790A=