Canonical Allele Identifier: CA1803221603
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780782A= , CM000670.2:g.93780782A= GRCh38
NC_000008.10:g.94793010A= , CM000670.1:g.94793010A= GRCh37
NC_000008.9:g.94862186A= NCBI36
NG_009190.1:g.30939A= , LRG_688:g.30939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.869+35A= ENSP00000314488.4:n.869+35A=
ENST00000409623.8:c.869+35A= ENSP00000386966.4:n.869+35A=
ENST00000452276.6:c.869+35A= ENSP00000388671.2:n.869+35A=
ENST00000453906.6:c.407-5441A= ENSP00000403035.2:n.407-5441A=
ENST00000520680.2:c.869+35A= ENSP00000428785.2:n.869+35A=
ENST00000521065.2:c.*586+35A= ENSP00000427947.2:n.*586+35A=
ENST00000521517.6:c.869+35A= ENSP00000430740.2:n.869+35A=
ENST00000681998.1:c.799+35A= ENSP00000506773.1:n.799+35A=
ENST00000682036.1:c.407-5441A= ENSP00000508390.1:n.407-5441A=
ENST00000682577.1:c.799+35A= ENSP00000506963.1:n.799+35A=
ENST00000682624.1:c.*443+35A= ENSP00000508343.1:n.*443+35A=
ENST00000682700.1:c.869+35A= ENSP00000507627.1:n.869+35A=
ENST00000682744.1:n.407+35A=
ENST00000682804.1:n.692+35A=
ENST00000682837.1:c.624+35A= ENSP00000507920.1:n.624+35A=
ENST00000682935.1:n.2429+35A=
ENST00000682984.1:c.530+35A= ENSP00000507209.1:n.530+35A=
ENST00000683078.1:c.624+35A= ENSP00000506796.1:n.624+35A=
ENST00000683223.1:c.710+35A= ENSP00000507685.1:n.710+35A=
ENST00000683238.1:n.2250+35A=
ENST00000683249.1:n.2450+35A=
ENST00000683336.1:c.799+35A= ENSP00000507695.1:n.799+35A=
ENST00000683362.1:c.530+35A= ENSP00000506985.1:n.530+35A=
ENST00000683850.1:n.792+35A=
ENST00000683919.1:c.799+35A= ENSP00000507617.1:n.799+35A=
ENST00000683953.1:c.780+35A= ENSP00000508375.1:n.780+35A=
ENST00000684023.1:c.1003+35A= ENSP00000507461.1:n.1003+35A=
ENST00000684064.1:c.560+35A= ENSP00000508192.1:n.560+35A=
ENST00000684089.1:n.2419+35A=
ENST00000684149.1:c.*205+35A= ENSP00000507943.1:n.*205+35A=
ENST00000684416.1:n.828+35A=
ENST00000684540.1:c.799+35A= ENSP00000507987.1:n.799+35A=
ENST00000453321.8:c.869+35A= MANE Select ENSP00000389998.3:n.869+35A=
ENST00000323130.7:c.839+35A= ENSP00000314488.3:n.839+35A=
ENST00000409623.7:c.626+35A= ENSP00000386966.3:n.626+35A=
ENST00000425545.2:n.316+35A=
ENST00000452276.5:c.560+35A= ENSP00000388671.1:n.560+35A=
ENST00000453321.7:c.869+35A= ENSP00000389998.3:n.869+35A=
ENST00000453906.5:c.407-5441A= ENSP00000403035.1:n.407-5441A=
ENST00000474944.5:n.427-5441A=
ENST00000496213.5:n.334+35A=
NM_001142301.1:c.626+35A= , LRG_688t2:c.626+35A= NP_001135773.1:n.626+35A=
NM_153704.5:c.869+35A= , LRG_688t1:c.869+35A= NP_714915.3:n.869+35A=
NR_024522.1:n.940+35A=
XM_006716686.2:c.566+35A= XP_006716749.1:n.566+35A=
XM_006716687.2:c.269+35A= XP_006716750.1:n.269+35A=
XM_011517363.1:c.407-5441A= XP_011515665.1:n.407-5441A=
XR_428387.1:n.927+35A=
XR_928360.1:n.927+35A=
XR_928361.1:n.927+35A=
XR_928362.1:n.927+35A=
XM_006716686.4:c.566+35A= XP_006716749.1:n.566+35A=
XM_011517363.3:c.407-5441A= XP_011515665.1:n.407-5441A=
XM_024447326.1:c.215+35A= XP_024303094.1:n.215+35A=
XR_001745619.2:n.910+35A=
XR_428387.2:n.910+35A=
XR_928360.3:n.910+35A=
XR_928362.3:n.910+35A=
NM_153704.6:c.869+35A= MANE Select NP_714915.3:n.869+35A=
NR_024522.2:n.890+35A=