Canonical Allele Identifier: CA1803211933
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93758401T= , CM000670.2:g.93758401T= GRCh38
NC_000008.10:g.94770629T= , CM000670.1:g.94770629T= GRCh37
NC_000008.9:g.94839805T= NCBI36
NG_009190.1:g.8558T= , LRG_688:g.8558T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.313-82T= ENSP00000314488.4:n.313-82T=
ENST00000409623.8:c.313-82T= ENSP00000386966.4:n.313-82T=
ENST00000452276.6:c.313-82T= ENSP00000388671.2:n.313-82T=
ENST00000453906.6:c.313-82T= ENSP00000403035.2:n.313-82T=
ENST00000520680.2:c.313-82T= ENSP00000428785.2:n.313-82T=
ENST00000521065.2:c.313-82T= ENSP00000427947.2:n.313-82T=
ENST00000521517.6:c.313-82T= ENSP00000430740.2:n.313-82T=
ENST00000681998.1:c.313-82T= ENSP00000506773.1:n.313-82T=
ENST00000682036.1:c.313-82T= ENSP00000508390.1:n.313-82T=
ENST00000682577.1:c.313-82T= ENSP00000506963.1:n.313-82T=
ENST00000682624.1:c.224-82T= ENSP00000508343.1:n.224-82T=
ENST00000682700.1:c.313-82T= ENSP00000507627.1:n.313-82T=
ENST00000682804.1:n.206-82T=
ENST00000682837.1:c.313-82T= ENSP00000507920.1:n.313-82T=
ENST00000682935.1:n.313-82T=
ENST00000682984.1:c.312+2535T= ENSP00000507209.1:n.312+2535T=
ENST00000683078.1:c.313-82T= ENSP00000506796.1:n.313-82T=
ENST00000683223.1:c.224-82T= ENSP00000507685.1:n.224-82T=
ENST00000683238.1:n.134-82T=
ENST00000683249.1:n.334-82T=
ENST00000683336.1:c.313-82T= ENSP00000507695.1:n.313-82T=
ENST00000683362.1:c.312+2535T= ENSP00000506985.1:n.312+2535T=
ENST00000683850.1:n.236-82T=
ENST00000683919.1:c.313-82T= ENSP00000507617.1:n.313-82T=
ENST00000683953.1:c.224-82T= ENSP00000508375.1:n.224-82T=
ENST00000684023.1:c.313-82T= ENSP00000507461.1:n.313-82T=
ENST00000684064.1:c.4-82T= ENSP00000508192.1:n.4-82T=
ENST00000684089.1:n.303-82T=
ENST00000684149.1:c.313-82T= ENSP00000507943.1:n.313-82T=
ENST00000684416.1:n.142-86T=
ENST00000684540.1:c.313-82T= ENSP00000507987.1:n.313-82T=
ENST00000684733.1:n.248-82T=
ENST00000453321.8:c.313-82T= MANE Select ENSP00000389998.3:n.313-82T=
ENST00000323130.7:c.283-82T= ENSP00000314488.3:n.283-82T=
ENST00000409623.7:c.-61-86T= ENSP00000386966.3:n.-61-86T=
ENST00000452276.5:c.4-82T= ENSP00000388671.1:n.4-82T=
ENST00000453321.7:c.313-82T= ENSP00000389998.3:n.313-82T=
ENST00000453906.5:c.313-82T= ENSP00000403035.1:n.313-82T=
ENST00000455946.5:c.313-82T= ENSP00000416339.1:n.313-82T=
ENST00000474944.5:n.333-82T=
ENST00000475305.1:n.322-82T=
ENST00000498673.5:c.-168-82T= ENSP00000430232.1:n.-168-82T=
ENST00000518319.5:c.-203-86T= ENSP00000430289.1:n.-203-86T=
ENST00000521065.1:c.219-82T=
ENST00000521222.5:c.313-86T= ENSP00000429925.1:n.313-86T=
ENST00000521517.5:c.305-82T=
NM_001142301.1:c.-61-86T= , LRG_688t2:c.-61-86T= NP_001135773.1:n.-61-86T=
NM_153704.5:c.313-82T= , LRG_688t1:c.313-82T= NP_714915.3:n.313-82T=
NR_024522.1:n.384-82T=
XM_006716686.2:c.10-82T= XP_006716749.1:n.10-82T=
XM_011517363.1:c.313-82T= XP_011515665.1:n.313-82T=
XR_428387.1:n.371-82T=
XR_928360.1:n.371-82T=
XR_928361.1:n.371-82T=
XR_928362.1:n.371-82T=
XM_006716686.4:c.10-82T= XP_006716749.1:n.10-82T=
XM_011517363.3:c.313-82T= XP_011515665.1:n.313-82T=
XM_024447326.1:c.-97-82T= XP_024303094.1:n.-97-82T=
XR_001745619.2:n.354-82T=
XR_428387.2:n.354-82T=
XR_928360.3:n.354-82T=
XR_928362.3:n.354-82T=
NM_153704.6:c.313-82T= MANE Select NP_714915.3:n.313-82T=
NR_024522.2:n.334-82T=