Canonical Allele Identifier: CA1803228180
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786328C= , CM000670.2:g.93786328C= GRCh38
NC_000008.10:g.94798556C= , CM000670.1:g.94798556C= GRCh37
NC_000008.9:g.94867732C= NCBI36
NG_009190.1:g.36485C= , LRG_688:g.36485C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1394C= ENSP00000314488.4:p.Ala465=
ENST00000409623.8:c.1349C= ENSP00000386966.4:p.Ala450=
ENST00000452276.6:c.1394C= ENSP00000388671.2:p.Ala465=
ENST00000453906.6:c.512C= ENSP00000403035.2:p.Ala171=
ENST00000520680.2:c.1394C= ENSP00000428785.2:p.Ala465=
ENST00000521517.6:c.1394C= ENSP00000430740.2:p.Ala465=
ENST00000681998.1:c.1215C= ENSP00000506773.1:n.1215C=
ENST00000682036.1:c.512C= ENSP00000508390.1:p.Ala171=
ENST00000682577.1:c.1167C= ENSP00000506963.1:n.1167C=
ENST00000682624.1:c.*968C= ENSP00000508343.1:n.*968C=
ENST00000682700.1:c.1394C= ENSP00000507627.1:p.Ala465=
ENST00000682744.1:n.932C=
ENST00000682804.1:n.1217C=
ENST00000682837.1:c.883C= ENSP00000507920.1:n.883C=
ENST00000682935.1:n.3444C=
ENST00000682984.1:c.1055C= ENSP00000507209.1:p.Ala352=
ENST00000683078.1:c.1149C= ENSP00000506796.1:n.1149C=
ENST00000683223.1:c.1126C= ENSP00000507685.1:n.1126C=
ENST00000683238.1:n.2618C=
ENST00000683249.1:n.2991C=
ENST00000683336.1:c.1215C= ENSP00000507695.1:n.1215C=
ENST00000683362.1:c.1055C= ENSP00000506985.1:p.Ala352=
ENST00000683850.1:n.1317C=
ENST00000683919.1:c.1324C= ENSP00000507617.1:n.1324C=
ENST00000683953.1:c.1305C= ENSP00000508375.1:n.1305C=
ENST00000684023.1:c.1371C= ENSP00000507461.1:n.1371C=
ENST00000684064.1:c.1085C= ENSP00000508192.1:p.Ala362=
ENST00000684089.1:n.2944C=
ENST00000684149.1:c.*573C= ENSP00000507943.1:n.*573C=
ENST00000684416.1:n.1353C=
ENST00000684540.1:c.1324C= ENSP00000507987.1:n.1324C=
ENST00000453321.8:c.1394C= MANE Select ENSP00000389998.3:p.Ala465=
ENST00000323130.7:c.1364C= ENSP00000314488.3:p.Ala455=
ENST00000409623.7:c.1151C= ENSP00000386966.3:p.Ala384=
ENST00000452276.5:c.1085C= ENSP00000388671.1:p.Ala362=
ENST00000453321.7:c.1394C= ENSP00000389998.3:p.Ala465=
ENST00000453906.5:c.512C= ENSP00000403035.1:p.Ala171=
ENST00000474944.5:n.532C=
ENST00000520680.1:c.216C=
NM_001142301.1:c.1151C= , LRG_688t2:c.1151C= NP_001135773.1:p.Ala384=
NM_153704.5:c.1394C= , LRG_688t1:c.1394C= NP_714915.3:p.Ala465=
NR_024522.1:n.1465C=
XM_006716686.2:c.1091C= XP_006716749.1:p.Ala364=
XM_006716687.2:c.794C= XP_006716750.1:p.Ala265=
XM_011517363.1:c.512C= XP_011515665.1:p.Ala171=
XR_428387.1:n.1452C=
XR_928360.1:n.1452C=
XR_928361.1:n.1452C=
XR_928362.1:n.1452C=
XM_006716686.4:c.1091C= XP_006716749.1:p.Ala364=
XM_011517363.3:c.512C= XP_011515665.1:p.Ala171=
XM_024447326.1:c.740C= XP_024303094.1:p.Ala247=
XR_001745619.2:n.1435C=
XR_428387.2:n.1435C=
XR_928360.3:n.1435C=
XR_928362.3:n.1435C=
NM_153704.6:c.1394C= MANE Select NP_714915.3:p.Ala465=
NR_024522.2:n.1415C=