Canonical Allele Identifier: CA371687795

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94792870T>C (hg19) ; chr8:g.93780642T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780642T>C , CM000670.2:g.93780642T>C	GRCh38
NC_000008.10:g.94792870T>C , CM000670.1:g.94792870T>C	GRCh37
NC_000008.9:g.94862046T>C	NCBI36
NG_009190.1:g.30799T>C , LRG_688:g.30799T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.764T>C	ENSP00000314488.4:p.Met255Thr
ENST00000409623.8:c.764T>C	ENSP00000386966.4:p.Met255Thr
ENST00000452276.6:c.764T>C	ENSP00000388671.2:p.Met255Thr
ENST00000453906.6:c.407-5581T>C	ENSP00000403035.2:n.407-5581T>C
ENST00000520680.2:c.764T>C	ENSP00000428785.2:p.Met255Thr
ENST00000521065.2:c.*481T>C	ENSP00000427947.2:n.*481T>C
ENST00000521517.6:c.764T>C	ENSP00000430740.2:p.Met255Thr
ENST00000681998.1:c.694T>C	ENSP00000506773.1:n.694T>C
ENST00000682036.1:c.407-5581T>C	ENSP00000508390.1:n.407-5581T>C
ENST00000682577.1:c.694T>C	ENSP00000506963.1:n.694T>C
ENST00000682624.1:c.*338T>C	ENSP00000508343.1:n.*338T>C
ENST00000682700.1:c.764T>C	ENSP00000507627.1:p.Met255Thr
ENST00000682744.1:n.302T>C
ENST00000682804.1:n.587T>C
ENST00000682837.1:c.519T>C	ENSP00000507920.1:p.Asp173=
ENST00000682935.1:n.2324T>C
ENST00000682984.1:c.425T>C	ENSP00000507209.1:p.Met142Thr
ENST00000683078.1:c.519T>C	ENSP00000506796.1:p.Asp173=
ENST00000683223.1:c.605T>C	ENSP00000507685.1:n.605T>C
ENST00000683238.1:n.2145T>C
ENST00000683249.1:n.2345T>C
ENST00000683336.1:c.694T>C	ENSP00000507695.1:n.694T>C
ENST00000683362.1:c.425T>C	ENSP00000506985.1:p.Met142Thr
ENST00000683850.1:n.687T>C
ENST00000683919.1:c.694T>C	ENSP00000507617.1:n.694T>C
ENST00000683953.1:c.675T>C	ENSP00000508375.1:n.675T>C
ENST00000684023.1:c.898T>C	ENSP00000507461.1:n.898T>C
ENST00000684064.1:c.455T>C	ENSP00000508192.1:p.Met152Thr
ENST00000684089.1:n.2314T>C
ENST00000684149.1:c.*100T>C	ENSP00000507943.1:n.*100T>C
ENST00000684416.1:n.723T>C
ENST00000684540.1:c.694T>C	ENSP00000507987.1:n.694T>C
ENST00000453321.8:c.764T>C MANE Select	ENSP00000389998.3:p.Met255Thr
ENST00000323130.7:c.734T>C	ENSP00000314488.3:p.Met245Thr
ENST00000409623.7:c.521T>C	ENSP00000386966.3:p.Met174Thr
ENST00000425545.2:n.211T>C
ENST00000452276.5:c.455T>C	ENSP00000388671.1:p.Met152Thr
ENST00000453321.7:c.764T>C	ENSP00000389998.3:p.Met255Thr
ENST00000453906.5:c.407-5581T>C	ENSP00000403035.1:n.407-5581T>C
ENST00000474944.5:n.427-5581T>C
ENST00000496213.5:n.229T>C
NM_001142301.1:c.521T>C , LRG_688t2:c.521T>C	NP_001135773.1:p.Met174Thr
NM_153704.5:c.764T>C , LRG_688t1:c.764T>C	NP_714915.3:p.Met255Thr
NR_024522.1:n.835T>C
XM_006716686.2:c.461T>C	XP_006716749.1:p.Met154Thr
XM_006716687.2:c.164T>C	XP_006716750.1:p.Met55Thr
XM_011517363.1:c.407-5581T>C	XP_011515665.1:n.407-5581T>C
XR_428387.1:n.822T>C
XR_928360.1:n.822T>C
XR_928361.1:n.822T>C
XR_928362.1:n.822T>C
XM_006716686.4:c.461T>C	XP_006716749.1:p.Met154Thr
XM_011517363.3:c.407-5581T>C	XP_011515665.1:n.407-5581T>C
XM_024447326.1:c.110T>C	XP_024303094.1:p.Met37Thr
XR_001745619.2:n.805T>C
XR_428387.2:n.805T>C
XR_928360.3:n.805T>C
XR_928362.3:n.805T>C
NM_153704.6:c.764T>C MANE Select	NP_714915.3:p.Met255Thr
NR_024522.2:n.785T>C