Canonical Allele Identifier: CA1803221059
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780544T= , CM000670.2:g.93780544T= GRCh38
NC_000008.10:g.94792772T= , CM000670.1:g.94792772T= GRCh37
NC_000008.9:g.94861948T= NCBI36
NG_009190.1:g.30701T= , LRG_688:g.30701T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.715-49T= ENSP00000314488.4:n.715-49T=
ENST00000409623.8:c.715-49T= ENSP00000386966.4:n.715-49T=
ENST00000452276.6:c.715-49T= ENSP00000388671.2:n.715-49T=
ENST00000453906.6:c.407-5679T= ENSP00000403035.2:n.407-5679T=
ENST00000520680.2:c.715-49T= ENSP00000428785.2:n.715-49T=
ENST00000521065.2:c.*432-49T= ENSP00000427947.2:n.*432-49T=
ENST00000521517.6:c.715-49T= ENSP00000430740.2:n.715-49T=
ENST00000681998.1:c.645-49T= ENSP00000506773.1:n.645-49T=
ENST00000682036.1:c.407-5679T= ENSP00000508390.1:n.407-5679T=
ENST00000682577.1:c.645-49T= ENSP00000506963.1:n.645-49T=
ENST00000682624.1:c.*289-49T= ENSP00000508343.1:n.*289-49T=
ENST00000682700.1:c.715-49T= ENSP00000507627.1:n.715-49T=
ENST00000682744.1:n.204T=
ENST00000682804.1:n.538-49T=
ENST00000682837.1:c.470-49T= ENSP00000507920.1:n.470-49T=
ENST00000682935.1:n.2275-49T=
ENST00000682984.1:c.376-49T= ENSP00000507209.1:n.376-49T=
ENST00000683078.1:c.470-49T= ENSP00000506796.1:n.470-49T=
ENST00000683223.1:c.556-49T= ENSP00000507685.1:n.556-49T=
ENST00000683238.1:n.2096-49T=
ENST00000683249.1:n.2296-49T=
ENST00000683336.1:c.645-49T= ENSP00000507695.1:n.645-49T=
ENST00000683362.1:c.376-49T= ENSP00000506985.1:n.376-49T=
ENST00000683850.1:n.638-49T=
ENST00000683919.1:c.645-49T= ENSP00000507617.1:n.645-49T=
ENST00000683953.1:c.626-49T= ENSP00000508375.1:n.626-49T=
ENST00000684023.1:c.849-49T= ENSP00000507461.1:n.849-49T=
ENST00000684064.1:c.406-49T= ENSP00000508192.1:n.406-49T=
ENST00000684089.1:n.2265-49T=
ENST00000684149.1:c.*51-49T= ENSP00000507943.1:n.*51-49T=
ENST00000684416.1:n.674-49T=
ENST00000684540.1:c.645-49T= ENSP00000507987.1:n.645-49T=
ENST00000453321.8:c.715-49T= MANE Select ENSP00000389998.3:n.715-49T=
ENST00000323130.7:c.685-49T= ENSP00000314488.3:n.685-49T=
ENST00000409623.7:c.472-49T= ENSP00000386966.3:n.472-49T=
ENST00000425545.2:n.162-49T=
ENST00000452276.5:c.406-49T= ENSP00000388671.1:n.406-49T=
ENST00000453321.7:c.715-49T= ENSP00000389998.3:n.715-49T=
ENST00000453906.5:c.407-5679T= ENSP00000403035.1:n.407-5679T=
ENST00000474944.5:n.427-5679T=
ENST00000496213.5:n.180-49T=
NM_001142301.1:c.472-49T= , LRG_688t2:c.472-49T= NP_001135773.1:n.472-49T=
NM_153704.5:c.715-49T= , LRG_688t1:c.715-49T= NP_714915.3:n.715-49T=
NR_024522.1:n.786-49T=
XM_006716686.2:c.412-49T= XP_006716749.1:n.412-49T=
XM_006716687.2:c.115-49T= XP_006716750.1:n.115-49T=
XM_011517363.1:c.407-5679T= XP_011515665.1:n.407-5679T=
XR_428387.1:n.773-49T=
XR_928360.1:n.773-49T=
XR_928361.1:n.773-49T=
XR_928362.1:n.773-49T=
XM_006716686.4:c.412-49T= XP_006716749.1:n.412-49T=
XM_011517363.3:c.407-5679T= XP_011515665.1:n.407-5679T=
XM_024447326.1:c.61-49T= XP_024303094.1:n.61-49T=
XR_001745619.2:n.756-49T=
XR_428387.2:n.756-49T=
XR_928360.3:n.756-49T=
XR_928362.3:n.756-49T=
NM_153704.6:c.715-49T= MANE Select NP_714915.3:n.715-49T=
NR_024522.2:n.736-49T=