Canonical Allele Identifier: CA1803237319
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93808802A= , CM000670.2:g.93808802A= GRCh38
NC_000008.10:g.94821030A= , CM000670.1:g.94821030A= GRCh37
NC_000008.9:g.94890206A= NCBI36
NG_009190.1:g.58959A= , LRG_688:g.58959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.2440-38A= ENSP00000314488.4:n.2440-38A=
ENST00000409623.8:c.2395-38A= ENSP00000386966.4:n.2395-38A=
ENST00000452276.6:c.2323-38A= ENSP00000388671.2:n.2323-38A=
ENST00000453906.6:c.1558-38A= ENSP00000403035.2:n.1558-38A=
ENST00000518896.2:c.731-38A= ENSP00000507992.1:n.731-38A=
ENST00000520680.2:c.2563-38A= ENSP00000428785.2:n.2563-38A=
ENST00000521517.6:c.2341-38A= ENSP00000430740.2:n.2341-38A=
ENST00000681998.1:c.2261-38A= ENSP00000506773.1:n.2261-38A=
ENST00000682036.1:c.1681-38A= ENSP00000508390.1:n.1681-38A=
ENST00000682577.1:c.2213-38A= ENSP00000506963.1:n.2213-38A=
ENST00000682624.1:c.*2014-38A= ENSP00000508343.1:n.*2014-38A=
ENST00000682700.1:c.2440-38A= ENSP00000507627.1:n.2440-38A=
ENST00000682744.1:n.1978-38A=
ENST00000682804.1:n.2263-38A=
ENST00000682837.1:c.1929-38A= ENSP00000507920.1:n.1929-38A=
ENST00000682935.1:n.4490-38A=
ENST00000682984.1:c.2101-38A= ENSP00000507209.1:n.2101-38A=
ENST00000683078.1:c.2195-38A= ENSP00000506796.1:n.2195-38A=
ENST00000683223.1:c.2172-38A= ENSP00000507685.1:n.2172-38A=
ENST00000683238.1:n.3664-38A=
ENST00000683249.1:n.4037-38A=
ENST00000683336.1:c.2261-38A= ENSP00000507695.1:n.2261-38A=
ENST00000683362.1:c.2101-38A= ENSP00000506985.1:n.2101-38A=
ENST00000683850.1:n.2363-38A=
ENST00000683919.1:c.2370-38A= ENSP00000507617.1:n.2370-38A=
ENST00000683953.1:c.2351-38A= ENSP00000508375.1:n.2351-38A=
ENST00000684023.1:c.2417-38A= ENSP00000507461.1:n.2417-38A=
ENST00000684064.1:c.2131-38A= ENSP00000508192.1:n.2131-38A=
ENST00000684089.1:n.3990-38A=
ENST00000684149.1:c.*1619-38A= ENSP00000507943.1:n.*1619-38A=
ENST00000684343.1:c.637-38A= ENSP00000507591.1:n.637-38A=
ENST00000684416.1:n.2399-38A=
ENST00000684540.1:c.2370-38A= ENSP00000507987.1:n.2370-38A=
ENST00000453321.8:c.2440-38A= MANE Select ENSP00000389998.3:n.2440-38A=
ENST00000323130.7:c.2410-38A= ENSP00000314488.3:n.2410-38A=
ENST00000409623.7:c.2197-38A= ENSP00000386966.3:n.2197-38A=
ENST00000453321.7:c.2440-38A= ENSP00000389998.3:n.2440-38A=
ENST00000474944.5:n.1578-38A=
ENST00000519845.5:n.1172-38A=
NM_001142301.1:c.2197-38A= , LRG_688t2:c.2197-38A= NP_001135773.1:n.2197-38A=
NM_153704.5:c.2440-38A= , LRG_688t1:c.2440-38A= NP_714915.3:n.2440-38A=
NR_024522.1:n.2511-38A=
XM_006716686.2:c.2137-38A= XP_006716749.1:n.2137-38A=
XM_006716687.2:c.1840-38A= XP_006716750.1:n.1840-38A=
XM_011517363.1:c.1558-38A= XP_011515665.1:n.1558-38A=
XR_428387.1:n.2498-38A=
XR_928360.1:n.2498-38A=
XR_928361.1:n.2498-38A=
XR_928362.1:n.2498-38A=
XM_006716686.4:c.2137-38A= XP_006716749.1:n.2137-38A=
XM_011517363.3:c.1558-38A= XP_011515665.1:n.1558-38A=
XM_024447326.1:c.1786-38A= XP_024303094.1:n.1786-38A=
XR_001745619.2:n.2481-38A=
XR_428387.2:n.2481-38A=
XR_928360.3:n.2481-38A=
XR_928362.3:n.2481-38A=
NM_153704.6:c.2440-38A= MANE Select NP_714915.3:n.2440-38A=
NR_024522.2:n.2461-38A=