Canonical Allele Identifier: CA1803221233
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780623C= , CM000670.2:g.93780623C= GRCh38
NC_000008.10:g.94792851C= , CM000670.1:g.94792851C= GRCh37
NC_000008.9:g.94862027C= NCBI36
NG_009190.1:g.30780C= , LRG_688:g.30780C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.745C= ENSP00000314488.4:p.Leu249=
ENST00000409623.8:c.745C= ENSP00000386966.4:p.Leu249=
ENST00000452276.6:c.745C= ENSP00000388671.2:p.Leu249=
ENST00000453906.6:c.407-5600C= ENSP00000403035.2:n.407-5600C=
ENST00000520680.2:c.745C= ENSP00000428785.2:p.Leu249=
ENST00000521065.2:c.*462C= ENSP00000427947.2:n.*462C=
ENST00000521517.6:c.745C= ENSP00000430740.2:p.Leu249=
ENST00000681998.1:c.675C= ENSP00000506773.1:n.675C=
ENST00000682036.1:c.407-5600C= ENSP00000508390.1:n.407-5600C=
ENST00000682577.1:c.675C= ENSP00000506963.1:n.675C=
ENST00000682624.1:c.*319C= ENSP00000508343.1:n.*319C=
ENST00000682700.1:c.745C= ENSP00000507627.1:p.Leu249=
ENST00000682744.1:n.283C=
ENST00000682804.1:n.568C=
ENST00000682837.1:c.500C= ENSP00000507920.1:p.Ser167=
ENST00000682935.1:n.2305C=
ENST00000682984.1:c.406C= ENSP00000507209.1:p.Leu136=
ENST00000683078.1:c.500C= ENSP00000506796.1:p.Ser167=
ENST00000683223.1:c.586C= ENSP00000507685.1:n.586C=
ENST00000683238.1:n.2126C=
ENST00000683249.1:n.2326C=
ENST00000683336.1:c.675C= ENSP00000507695.1:n.675C=
ENST00000683362.1:c.406C= ENSP00000506985.1:p.Leu136=
ENST00000683850.1:n.668C=
ENST00000683919.1:c.675C= ENSP00000507617.1:n.675C=
ENST00000683953.1:c.656C= ENSP00000508375.1:n.656C=
ENST00000684023.1:c.879C= ENSP00000507461.1:n.879C=
ENST00000684064.1:c.436C= ENSP00000508192.1:p.Leu146=
ENST00000684089.1:n.2295C=
ENST00000684149.1:c.*81C= ENSP00000507943.1:n.*81C=
ENST00000684416.1:n.704C=
ENST00000684540.1:c.675C= ENSP00000507987.1:n.675C=
ENST00000453321.8:c.745C= MANE Select ENSP00000389998.3:p.Leu249=
ENST00000323130.7:c.715C= ENSP00000314488.3:p.Leu239=
ENST00000409623.7:c.502C= ENSP00000386966.3:p.Leu168=
ENST00000425545.2:n.192C=
ENST00000452276.5:c.436C= ENSP00000388671.1:p.Leu146=
ENST00000453321.7:c.745C= ENSP00000389998.3:p.Leu249=
ENST00000453906.5:c.407-5600C= ENSP00000403035.1:n.407-5600C=
ENST00000474944.5:n.427-5600C=
ENST00000496213.5:n.210C=
NM_001142301.1:c.502C= , LRG_688t2:c.502C= NP_001135773.1:p.Leu168=
NM_153704.5:c.745C= , LRG_688t1:c.745C= NP_714915.3:p.Leu249=
NR_024522.1:n.816C=
XM_006716686.2:c.442C= XP_006716749.1:p.Leu148=
XM_006716687.2:c.145C= XP_006716750.1:p.Leu49=
XM_011517363.1:c.407-5600C= XP_011515665.1:n.407-5600C=
XR_428387.1:n.803C=
XR_928360.1:n.803C=
XR_928361.1:n.803C=
XR_928362.1:n.803C=
XM_006716686.4:c.442C= XP_006716749.1:p.Leu148=
XM_011517363.3:c.407-5600C= XP_011515665.1:n.407-5600C=
XM_024447326.1:c.91C= XP_024303094.1:p.Leu31=
XR_001745619.2:n.786C=
XR_428387.2:n.786C=
XR_928360.3:n.786C=
XR_928362.3:n.786C=
NM_153704.6:c.745C= MANE Select NP_714915.3:p.Leu249=
NR_024522.2:n.766C=