Canonical Allele Identifier: CA2579206030
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93809022del , CM000670.2:g.93809022del GRCh38
NC_000008.10:g.94821250del , CM000670.1:g.94821250del GRCh37
NC_000008.9:g.94890426del NCBI36
NG_009190.1:g.59179del , LRG_688:g.59179del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.2557-35del ENSP00000314488.4:n.2557-35del
ENST00000409623.8:c.2512-35del ENSP00000386966.4:n.2512-35del
ENST00000452276.6:c.2440-35del ENSP00000388671.2:n.2440-35del
ENST00000453906.6:c.1675-35del ENSP00000403035.2:n.1675-35del
ENST00000518896.2:c.848-35del ENSP00000507992.1:n.848-35del
ENST00000520680.2:c.2680-35del ENSP00000428785.2:n.2680-35del
ENST00000521517.6:c.2458-35del ENSP00000430740.2:n.2458-35del
ENST00000681998.1:c.2378-35del ENSP00000506773.1:n.2378-35del
ENST00000682036.1:c.1798-35del ENSP00000508390.1:n.1798-35del
ENST00000682577.1:c.2330-35del ENSP00000506963.1:n.2330-35del
ENST00000682624.1:c.*2131-35del ENSP00000508343.1:n.*2131-35del
ENST00000682700.1:c.2557-35del ENSP00000507627.1:n.2557-35del
ENST00000682744.1:n.2095-35del
ENST00000682804.1:n.2380-35del
ENST00000682837.1:c.2046-35del ENSP00000507920.1:n.2046-35del
ENST00000682935.1:n.4607-35del
ENST00000682984.1:c.2218-35del ENSP00000507209.1:n.2218-35del
ENST00000683078.1:c.2312-35del ENSP00000506796.1:n.2312-35del
ENST00000683223.1:c.2289-35del ENSP00000507685.1:n.2289-35del
ENST00000683238.1:n.3781-35del
ENST00000683249.1:n.4154-35del
ENST00000683336.1:c.2378-35del ENSP00000507695.1:n.2378-35del
ENST00000683362.1:c.2218-35del ENSP00000506985.1:n.2218-35del
ENST00000683850.1:n.2480-35del
ENST00000683919.1:c.2487-35del ENSP00000507617.1:n.2487-35del
ENST00000683953.1:c.2468-35del ENSP00000508375.1:n.2468-35del
ENST00000684023.1:c.2534-35del ENSP00000507461.1:n.2534-35del
ENST00000684064.1:c.2248-35del ENSP00000508192.1:n.2248-35del
ENST00000684089.1:n.4107-35del
ENST00000684149.1:c.*1736-35del ENSP00000507943.1:n.*1736-35del
ENST00000684343.1:c.754-35del ENSP00000507591.1:n.754-35del
ENST00000684416.1:n.2516-35del
ENST00000684540.1:c.2487-35del ENSP00000507987.1:n.2487-35del
ENST00000453321.8:c.2557-35del MANE Select ENSP00000389998.3:n.2557-35del
ENST00000323130.7:c.2527-35del ENSP00000314488.3:n.2527-35del
ENST00000409623.7:c.2314-35del ENSP00000386966.3:n.2314-35del
ENST00000453321.7:c.2557-35del ENSP00000389998.3:n.2557-35del
ENST00000474944.5:n.1695-35del
ENST00000519845.5:n.1289-35del
NM_001142301.1:c.2314-35del , LRG_688t2:c.2314-35del NP_001135773.1:n.2314-35del
NM_153704.5:c.2557-35del , LRG_688t1:c.2557-35del NP_714915.3:n.2557-35del
NR_024522.1:n.2628-35del
XM_006716686.2:c.2254-35del XP_006716749.1:n.2254-35del
XM_006716687.2:c.1957-35del XP_006716750.1:n.1957-35del
XM_011517363.1:c.1675-35del XP_011515665.1:n.1675-35del
XR_428387.1:n.2615-35del
XR_928360.1:n.2615-35del
XR_928361.1:n.2615-35del
XR_928362.1:n.2615-35del
XM_006716686.4:c.2254-35del XP_006716749.1:n.2254-35del
XM_011517363.3:c.1675-35del XP_011515665.1:n.1675-35del
XM_024447326.1:c.1903-35del XP_024303094.1:n.1903-35del
XR_001745619.2:n.2598-35del
XR_428387.2:n.2598-35del
XR_928360.3:n.2598-35del
XR_928362.3:n.2598-35del
NM_153704.6:c.2557-35del MANE Select NP_714915.3:n.2557-35del
NR_024522.2:n.2578-35del