Canonical Allele Identifier: CA1803228027
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93786280G= , CM000670.2:g.93786280G= GRCh38
NC_000008.10:g.94798508G= , CM000670.1:g.94798508G= GRCh37
NC_000008.9:g.94867684G= NCBI36
NG_009190.1:g.36437G= , LRG_688:g.36437G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.1346G= ENSP00000314488.4:p.Ser449=
ENST00000409623.8:c.1301G= ENSP00000386966.4:p.Ser434=
ENST00000452276.6:c.1346G= ENSP00000388671.2:p.Ser449=
ENST00000453906.6:c.464G= ENSP00000403035.2:p.Ser155=
ENST00000520680.2:c.1346G= ENSP00000428785.2:p.Ser449=
ENST00000521517.6:c.1346G= ENSP00000430740.2:p.Ser449=
ENST00000681998.1:c.1167G= ENSP00000506773.1:n.1167G=
ENST00000682036.1:c.464G= ENSP00000508390.1:p.Ser155=
ENST00000682577.1:c.1119G= ENSP00000506963.1:n.1119G=
ENST00000682624.1:c.*920G= ENSP00000508343.1:n.*920G=
ENST00000682700.1:c.1346G= ENSP00000507627.1:p.Ser449=
ENST00000682744.1:n.884G=
ENST00000682804.1:n.1169G=
ENST00000682837.1:c.835G= ENSP00000507920.1:n.835G=
ENST00000682935.1:n.3396G=
ENST00000682984.1:c.1007G= ENSP00000507209.1:p.Ser336=
ENST00000683078.1:c.1101G= ENSP00000506796.1:n.1101G=
ENST00000683223.1:c.1078G= ENSP00000507685.1:n.1078G=
ENST00000683238.1:n.2570G=
ENST00000683249.1:n.2943G=
ENST00000683336.1:c.1167G= ENSP00000507695.1:n.1167G=
ENST00000683362.1:c.1007G= ENSP00000506985.1:p.Ser336=
ENST00000683850.1:n.1269G=
ENST00000683919.1:c.1276G= ENSP00000507617.1:n.1276G=
ENST00000683953.1:c.1257G= ENSP00000508375.1:n.1257G=
ENST00000684023.1:c.1323G= ENSP00000507461.1:n.1323G=
ENST00000684064.1:c.1037G= ENSP00000508192.1:p.Ser346=
ENST00000684089.1:n.2896G=
ENST00000684149.1:c.*525G= ENSP00000507943.1:n.*525G=
ENST00000684416.1:n.1305G=
ENST00000684540.1:c.1276G= ENSP00000507987.1:n.1276G=
ENST00000453321.8:c.1346G= MANE Select ENSP00000389998.3:p.Ser449=
ENST00000323130.7:c.1316G= ENSP00000314488.3:p.Ser439=
ENST00000409623.7:c.1103G= ENSP00000386966.3:p.Ser368=
ENST00000452276.5:c.1037G= ENSP00000388671.1:p.Ser346=
ENST00000453321.7:c.1346G= ENSP00000389998.3:p.Ser449=
ENST00000453906.5:c.464G= ENSP00000403035.1:p.Ser155=
ENST00000474944.5:n.484G=
ENST00000520680.1:c.168G=
NM_001142301.1:c.1103G= , LRG_688t2:c.1103G= NP_001135773.1:p.Ser368=
NM_153704.5:c.1346G= , LRG_688t1:c.1346G= NP_714915.3:p.Ser449=
NR_024522.1:n.1417G=
XM_006716686.2:c.1043G= XP_006716749.1:p.Ser348=
XM_006716687.2:c.746G= XP_006716750.1:p.Ser249=
XM_011517363.1:c.464G= XP_011515665.1:p.Ser155=
XR_428387.1:n.1404G=
XR_928360.1:n.1404G=
XR_928361.1:n.1404G=
XR_928362.1:n.1404G=
XM_006716686.4:c.1043G= XP_006716749.1:p.Ser348=
XM_011517363.3:c.464G= XP_011515665.1:p.Ser155=
XM_024447326.1:c.692G= XP_024303094.1:p.Ser231=
XR_001745619.2:n.1387G=
XR_428387.2:n.1387G=
XR_928360.3:n.1387G=
XR_928362.3:n.1387G=
NM_153704.6:c.1346G= MANE Select NP_714915.3:p.Ser449=
NR_024522.2:n.1367G=