Canonical Allele Identifier: CA1803221762
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780866_93780867delinsGT , CM000670.2:g.93780866_93780867delinsGT GRCh38
NC_000008.10:g.94793094_94793095delinsGT , CM000670.1:g.94793094_94793095delinsGT GRCh37
NC_000008.9:g.94862270_94862271delinsGT NCBI36
NG_009190.1:g.31023_31024delinsGT , LRG_688:g.31023_31024delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000323130.8:c.870-8_870-7delinsGT ENSP00000314488.4:n.870-8_870-7delinsGT
ENST00000409623.8:c.870-8_870-7delinsGT ENSP00000386966.4:n.870-8_870-7delinsGT
ENST00000452276.6:c.870-8_870-7delinsGT ENSP00000388671.2:n.870-8_870-7delinsGT
ENST00000453906.6:c.407-5357_407-5356delinsGT ENSP00000403035.2:n.407-5357_407-5356deli...
ENST00000520680.2:c.870-8_870-7delinsGT ENSP00000428785.2:n.870-8_870-7delinsGT
ENST00000521065.2:c.*587-8_*587-7delinsGT ENSP00000427947.2:n.*587-8_*587-7delinsGT...
ENST00000521517.6:c.870-8_870-7delinsGT ENSP00000430740.2:n.870-8_870-7delinsGT
ENST00000681998.1:c.799+119_799+120delinsGT ENSP00000506773.1:n.799+119_799+120delins...
ENST00000682036.1:c.407-5357_407-5356delinsGT ENSP00000508390.1:n.407-5357_407-5356deli...
ENST00000682577.1:c.800-8_800-7delinsGT ENSP00000506963.1:n.800-8_800-7delinsGT
ENST00000682624.1:c.*444-8_*444-7delinsGT ENSP00000508343.1:n.*444-8_*444-7delinsGT...
ENST00000682700.1:c.870-8_870-7delinsGT ENSP00000507627.1:n.870-8_870-7delinsGT
ENST00000682744.1:n.408-8_408-7delinsGT
ENST00000682804.1:n.693-8_693-7delinsGT
ENST00000682837.1:c.624+119_624+120delinsGT ENSP00000507920.1:n.624+119_624+120delins...
ENST00000682935.1:n.2430-8_2430-7delinsGT
ENST00000682984.1:c.531-8_531-7delinsGT ENSP00000507209.1:n.531-8_531-7delinsGT
ENST00000683078.1:c.625-8_625-7delinsGT ENSP00000506796.1:n.625-8_625-7delinsGT
ENST00000683223.1:c.710+119_710+120delinsGT ENSP00000507685.1:n.710+119_710+120delins...
ENST00000683238.1:n.2251-8_2251-7delinsGT
ENST00000683249.1:n.2459_2460delinsGT
ENST00000683336.1:c.799+119_799+120delinsGT ENSP00000507695.1:n.799+119_799+120delins...
ENST00000683362.1:c.531-8_531-7delinsGT ENSP00000506985.1:n.531-8_531-7delinsGT
ENST00000683850.1:n.793-8_793-7delinsGT
ENST00000683919.1:c.800-8_800-7delinsGT ENSP00000507617.1:n.800-8_800-7delinsGT
ENST00000683953.1:c.781-8_781-7delinsGT ENSP00000508375.1:n.781-8_781-7delinsGT
ENST00000684023.1:c.1004-8_1004-7delinsGT ENSP00000507461.1:n.1004-8_1004-7delinsGT...
ENST00000684064.1:c.561-8_561-7delinsGT ENSP00000508192.1:n.561-8_561-7delinsGT
ENST00000684089.1:n.2420-8_2420-7delinsGT
ENST00000684149.1:c.*206-8_*206-7delinsGT ENSP00000507943.1:n.*206-8_*206-7delinsGT...
ENST00000684416.1:n.829-8_829-7delinsGT
ENST00000684540.1:c.800-8_800-7delinsGT ENSP00000507987.1:n.800-8_800-7delinsGT
ENST00000453321.8:c.870-8_870-7delinsGT MANE Select ENSP00000389998.3:n.870-8_870-7delinsGT
ENST00000323130.7:c.840-8_840-7delinsGT ENSP00000314488.3:n.840-8_840-7delinsGT
ENST00000409623.7:c.627-8_627-7delinsGT ENSP00000386966.3:n.627-8_627-7delinsGT
ENST00000425545.2:n.317-8_317-7delinsGT
ENST00000452276.5:c.561-8_561-7delinsGT ENSP00000388671.1:n.561-8_561-7delinsGT
ENST00000453321.7:c.870-8_870-7delinsGT ENSP00000389998.3:n.870-8_870-7delinsGT
ENST00000453906.5:c.407-5357_407-5356delinsGT ENSP00000403035.1:n.407-5357_407-5356deli...
ENST00000474944.5:n.427-5357_427-5356delinsGT
ENST00000496213.5:n.335-8_335-7delinsGT
NM_001142301.1:c.627-8_627-7delinsGT , LRG_688t2:c.627-8_627-7delinsGT NP_001135773.1:n.627-8_627-7delinsGT
NM_153704.5:c.870-8_870-7delinsGT , LRG_688t1:c.870-8_870-7delinsGT NP_714915.3:n.870-8_870-7delinsGT
NR_024522.1:n.941-8_941-7delinsGT
XM_006716686.2:c.567-8_567-7delinsGT XP_006716749.1:n.567-8_567-7delinsGT
XM_006716687.2:c.270-8_270-7delinsGT XP_006716750.1:n.270-8_270-7delinsGT
XM_011517363.1:c.407-5357_407-5356delinsGT XP_011515665.1:n.407-5357_407-5356delinsG...
XR_428387.1:n.928-8_928-7delinsGT
XR_928360.1:n.928-8_928-7delinsGT
XR_928361.1:n.928-8_928-7delinsGT
XR_928362.1:n.928-8_928-7delinsGT
XM_006716686.4:c.567-8_567-7delinsGT XP_006716749.1:n.567-8_567-7delinsGT
XM_011517363.3:c.407-5357_407-5356delinsGT XP_011515665.1:n.407-5357_407-5356delinsG...
XM_024447326.1:c.216-8_216-7delinsGT XP_024303094.1:n.216-8_216-7delinsGT
XR_001745619.2:n.911-8_911-7delinsGT
XR_428387.2:n.911-8_911-7delinsGT
XR_928360.3:n.911-8_911-7delinsGT
XR_928362.3:n.911-8_911-7delinsGT
NM_153704.6:c.870-8_870-7delinsGT MANE Select NP_714915.3:n.870-8_870-7delinsGT
NR_024522.2:n.891-8_891-7delinsGT