Canonical Allele Identifier: CA1803226513
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93803576T= , CM000670.2:g.93803576T= GRCh38
NC_000008.10:g.94815804T= , CM000670.1:g.94815804T= GRCh37
NC_000008.9:g.94884980T= NCBI36
NG_009190.1:g.53733T= , LRG_688:g.53733T=

Transcript Alleles

HGVS Amino-acid change
ENST00000323130.8:c.2242-28T= ENSP00000314488.4:n.2242-28T=
ENST00000409623.8:c.2197-28T= ENSP00000386966.4:n.2197-28T=
ENST00000452276.6:c.2242-28T= ENSP00000388671.2:n.2242-28T=
ENST00000453906.6:c.1360-28T= ENSP00000403035.2:n.1360-28T=
ENST00000518896.2:c.533-28T= ENSP00000507992.1:n.533-28T=
ENST00000520680.2:c.2365-28T= ENSP00000428785.2:n.2365-28T=
ENST00000521517.6:c.2143-28T= ENSP00000430740.2:n.2143-28T=
ENST00000681998.1:c.2063-28T= ENSP00000506773.1:n.2063-28T=
ENST00000682036.1:c.1483-28T= ENSP00000508390.1:n.1483-28T=
ENST00000682577.1:c.2015-28T= ENSP00000506963.1:n.2015-28T=
ENST00000682624.1:c.*1816-28T= ENSP00000508343.1:n.*1816-28T=
ENST00000682700.1:c.2242-28T= ENSP00000507627.1:n.2242-28T=
ENST00000682744.1:n.1780-28T=
ENST00000682804.1:n.2065-28T=
ENST00000682837.1:c.1731-28T= ENSP00000507920.1:n.1731-28T=
ENST00000682935.1:n.4292-28T=
ENST00000682984.1:c.1903-28T= ENSP00000507209.1:n.1903-28T=
ENST00000683078.1:c.1997-28T= ENSP00000506796.1:n.1997-28T=
ENST00000683223.1:c.1974-28T= ENSP00000507685.1:n.1974-28T=
ENST00000683238.1:n.3466-28T=
ENST00000683249.1:n.3839-28T=
ENST00000683336.1:c.2063-28T= ENSP00000507695.1:n.2063-28T=
ENST00000683362.1:c.1903-28T= ENSP00000506985.1:n.1903-28T=
ENST00000683850.1:n.2165-28T=
ENST00000683919.1:c.2172-28T= ENSP00000507617.1:n.2172-28T=
ENST00000683953.1:c.2153-28T= ENSP00000508375.1:n.2153-28T=
ENST00000684023.1:c.2219-28T= ENSP00000507461.1:n.2219-28T=
ENST00000684064.1:c.1933-28T= ENSP00000508192.1:n.1933-28T=
ENST00000684089.1:n.3792-28T=
ENST00000684149.1:c.*1421-28T= ENSP00000507943.1:n.*1421-28T=
ENST00000684343.1:c.439-28T= ENSP00000507591.1:n.439-28T=
ENST00000684416.1:n.2201-28T=
ENST00000684540.1:c.2172-28T= ENSP00000507987.1:n.2172-28T=
ENST00000453321.8:c.2242-28T= MANE Select ENSP00000389998.3:n.2242-28T=
ENST00000323130.7:c.2212-28T= ENSP00000314488.3:n.2212-28T=
ENST00000409623.7:c.1999-28T= ENSP00000386966.3:n.1999-28T=
ENST00000453321.7:c.2242-28T= ENSP00000389998.3:n.2242-28T=
ENST00000474944.5:n.1380-28T=
ENST00000519845.5:n.974-28T=
NM_001142301.1:c.1999-28T= , LRG_688t2:c.1999-28T= NP_001135773.1:n.1999-28T=
NM_153704.5:c.2242-28T= , LRG_688t1:c.2242-28T= NP_714915.3:n.2242-28T=
NR_024522.1:n.2313-28T=
XM_006716686.2:c.1939-28T= XP_006716749.1:n.1939-28T=
XM_006716687.2:c.1642-28T= XP_006716750.1:n.1642-28T=
XM_011517363.1:c.1360-28T= XP_011515665.1:n.1360-28T=
XR_428387.1:n.2300-28T=
XR_928360.1:n.2300-28T=
XR_928361.1:n.2300-28T=
XR_928362.1:n.2300-28T=
XM_006716686.4:c.1939-28T= XP_006716749.1:n.1939-28T=
XM_011517363.3:c.1360-28T= XP_011515665.1:n.1360-28T=
XM_024447326.1:c.1588-28T= XP_024303094.1:n.1588-28T=
XR_001745619.2:n.2283-28T=
XR_428387.2:n.2283-28T=
XR_928360.3:n.2283-28T=
XR_928362.3:n.2283-28T=
NM_153704.6:c.2242-28T= MANE Select NP_714915.3:n.2242-28T=
NR_024522.2:n.2263-28T=