Canonical Allele Identifier: CA1803220952
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93780448C= , CM000670.2:g.93780448C= GRCh38
NC_000008.10:g.94792676C= , CM000670.1:g.94792676C= GRCh37
NC_000008.9:g.94861852C= NCBI36
NG_009190.1:g.30605C= , LRG_688:g.30605C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.715-145C= ENSP00000314488.4:n.715-145C=
ENST00000409623.8:c.715-145C= ENSP00000386966.4:n.715-145C=
ENST00000452276.6:c.715-145C= ENSP00000388671.2:n.715-145C=
ENST00000453906.6:c.407-5775C= ENSP00000403035.2:n.407-5775C=
ENST00000520680.2:c.715-145C= ENSP00000428785.2:n.715-145C=
ENST00000521065.2:c.*432-145C= ENSP00000427947.2:n.*432-145C=
ENST00000521517.6:c.715-145C= ENSP00000430740.2:n.715-145C=
ENST00000681998.1:c.645-145C= ENSP00000506773.1:n.645-145C=
ENST00000682036.1:c.407-5775C= ENSP00000508390.1:n.407-5775C=
ENST00000682577.1:c.645-145C= ENSP00000506963.1:n.645-145C=
ENST00000682624.1:c.*289-145C= ENSP00000508343.1:n.*289-145C=
ENST00000682700.1:c.715-145C= ENSP00000507627.1:n.715-145C=
ENST00000682744.1:n.108C=
ENST00000682804.1:n.538-145C=
ENST00000682837.1:c.470-145C= ENSP00000507920.1:n.470-145C=
ENST00000682935.1:n.2275-145C=
ENST00000682984.1:c.376-145C= ENSP00000507209.1:n.376-145C=
ENST00000683078.1:c.470-145C= ENSP00000506796.1:n.470-145C=
ENST00000683223.1:c.556-145C= ENSP00000507685.1:n.556-145C=
ENST00000683238.1:n.2096-145C=
ENST00000683249.1:n.2296-145C=
ENST00000683336.1:c.645-145C= ENSP00000507695.1:n.645-145C=
ENST00000683362.1:c.376-145C= ENSP00000506985.1:n.376-145C=
ENST00000683850.1:n.638-145C=
ENST00000683919.1:c.645-145C= ENSP00000507617.1:n.645-145C=
ENST00000683953.1:c.626-145C= ENSP00000508375.1:n.626-145C=
ENST00000684023.1:c.849-145C= ENSP00000507461.1:n.849-145C=
ENST00000684064.1:c.406-145C= ENSP00000508192.1:n.406-145C=
ENST00000684089.1:n.2265-145C=
ENST00000684149.1:c.*51-145C= ENSP00000507943.1:n.*51-145C=
ENST00000684416.1:n.674-145C=
ENST00000684540.1:c.645-145C= ENSP00000507987.1:n.645-145C=
ENST00000453321.8:c.715-145C= MANE Select ENSP00000389998.3:n.715-145C=
ENST00000323130.7:c.685-145C= ENSP00000314488.3:n.685-145C=
ENST00000409623.7:c.472-145C= ENSP00000386966.3:n.472-145C=
ENST00000425545.2:n.162-145C=
ENST00000452276.5:c.406-145C= ENSP00000388671.1:n.406-145C=
ENST00000453321.7:c.715-145C= ENSP00000389998.3:n.715-145C=
ENST00000453906.5:c.407-5775C= ENSP00000403035.1:n.407-5775C=
ENST00000474944.5:n.427-5775C=
ENST00000496213.5:n.180-145C=
NM_001142301.1:c.472-145C= , LRG_688t2:c.472-145C= NP_001135773.1:n.472-145C=
NM_153704.5:c.715-145C= , LRG_688t1:c.715-145C= NP_714915.3:n.715-145C=
NR_024522.1:n.786-145C=
XM_006716686.2:c.412-145C= XP_006716749.1:n.412-145C=
XM_006716687.2:c.115-145C= XP_006716750.1:n.115-145C=
XM_011517363.1:c.407-5775C= XP_011515665.1:n.407-5775C=
XR_428387.1:n.773-145C=
XR_928360.1:n.773-145C=
XR_928361.1:n.773-145C=
XR_928362.1:n.773-145C=
XM_006716686.4:c.412-145C= XP_006716749.1:n.412-145C=
XM_011517363.3:c.407-5775C= XP_011515665.1:n.407-5775C=
XM_024447326.1:c.61-145C= XP_024303094.1:n.61-145C=
XR_001745619.2:n.756-145C=
XR_428387.2:n.756-145C=
XR_928360.3:n.756-145C=
XR_928362.3:n.756-145C=
NM_153704.6:c.715-145C= MANE Select NP_714915.3:n.715-145C=
NR_024522.2:n.736-145C=