Canonical Allele Identifier: CA371689825

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94798547T>C (hg19) ; chr8:g.93786319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93786319T>C , CM000670.2:g.93786319T>C	GRCh38
NC_000008.10:g.94798547T>C , CM000670.1:g.94798547T>C	GRCh37
NC_000008.9:g.94867723T>C	NCBI36
NG_009190.1:g.36476T>C , LRG_688:g.36476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.1385T>C	ENSP00000314488.4:p.Ile462Thr
ENST00000409623.8:c.1340T>C	ENSP00000386966.4:p.Ile447Thr
ENST00000452276.6:c.1385T>C	ENSP00000388671.2:p.Ile462Thr
ENST00000453906.6:c.503T>C	ENSP00000403035.2:p.Ile168Thr
ENST00000520680.2:c.1385T>C	ENSP00000428785.2:p.Ile462Thr
ENST00000521517.6:c.1385T>C	ENSP00000430740.2:p.Ile462Thr
ENST00000681998.1:c.1206T>C	ENSP00000506773.1:n.1206T>C
ENST00000682036.1:c.503T>C	ENSP00000508390.1:p.Ile168Thr
ENST00000682577.1:c.1158T>C	ENSP00000506963.1:n.1158T>C
ENST00000682624.1:c.*959T>C	ENSP00000508343.1:n.*959T>C
ENST00000682700.1:c.1385T>C	ENSP00000507627.1:p.Ile462Thr
ENST00000682744.1:n.923T>C
ENST00000682804.1:n.1208T>C
ENST00000682837.1:c.874T>C	ENSP00000507920.1:n.874T>C
ENST00000682935.1:n.3435T>C
ENST00000682984.1:c.1046T>C	ENSP00000507209.1:p.Ile349Thr
ENST00000683078.1:c.1140T>C	ENSP00000506796.1:n.1140T>C
ENST00000683223.1:c.1117T>C	ENSP00000507685.1:n.1117T>C
ENST00000683238.1:n.2609T>C
ENST00000683249.1:n.2982T>C
ENST00000683336.1:c.1206T>C	ENSP00000507695.1:n.1206T>C
ENST00000683362.1:c.1046T>C	ENSP00000506985.1:p.Ile349Thr
ENST00000683850.1:n.1308T>C
ENST00000683919.1:c.1315T>C	ENSP00000507617.1:n.1315T>C
ENST00000683953.1:c.1296T>C	ENSP00000508375.1:n.1296T>C
ENST00000684023.1:c.1362T>C	ENSP00000507461.1:n.1362T>C
ENST00000684064.1:c.1076T>C	ENSP00000508192.1:p.Ile359Thr
ENST00000684089.1:n.2935T>C
ENST00000684149.1:c.*564T>C	ENSP00000507943.1:n.*564T>C
ENST00000684416.1:n.1344T>C
ENST00000684540.1:c.1315T>C	ENSP00000507987.1:n.1315T>C
ENST00000453321.8:c.1385T>C MANE Select	ENSP00000389998.3:p.Ile462Thr
ENST00000323130.7:c.1355T>C	ENSP00000314488.3:p.Ile452Thr
ENST00000409623.7:c.1142T>C	ENSP00000386966.3:p.Ile381Thr
ENST00000452276.5:c.1076T>C	ENSP00000388671.1:p.Ile359Thr
ENST00000453321.7:c.1385T>C	ENSP00000389998.3:p.Ile462Thr
ENST00000453906.5:c.503T>C	ENSP00000403035.1:p.Ile168Thr
ENST00000474944.5:n.523T>C
ENST00000520680.1:c.207T>C
NM_001142301.1:c.1142T>C , LRG_688t2:c.1142T>C	NP_001135773.1:p.Ile381Thr
NM_153704.5:c.1385T>C , LRG_688t1:c.1385T>C	NP_714915.3:p.Ile462Thr
NR_024522.1:n.1456T>C
XM_006716686.2:c.1082T>C	XP_006716749.1:p.Ile361Thr
XM_006716687.2:c.785T>C	XP_006716750.1:p.Ile262Thr
XM_011517363.1:c.503T>C	XP_011515665.1:p.Ile168Thr
XR_428387.1:n.1443T>C
XR_928360.1:n.1443T>C
XR_928361.1:n.1443T>C
XR_928362.1:n.1443T>C
XM_006716686.4:c.1082T>C	XP_006716749.1:p.Ile361Thr
XM_011517363.3:c.503T>C	XP_011515665.1:p.Ile168Thr
XM_024447326.1:c.731T>C	XP_024303094.1:p.Ile244Thr
XR_001745619.2:n.1426T>C
XR_428387.2:n.1426T>C
XR_928360.3:n.1426T>C
XR_928362.3:n.1426T>C
NM_153704.6:c.1385T>C MANE Select	NP_714915.3:p.Ile462Thr
NR_024522.2:n.1406T>C