Canonical Allele Identifier: CA371687752

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94792849C>G (hg19) ; chr8:g.93780621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780621C>G , CM000670.2:g.93780621C>G	GRCh38
NC_000008.10:g.94792849C>G , CM000670.1:g.94792849C>G	GRCh37
NC_000008.9:g.94862025C>G	NCBI36
NG_009190.1:g.30778C>G , LRG_688:g.30778C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.743C>G	ENSP00000314488.4:p.Ala248Gly
ENST00000409623.8:c.743C>G	ENSP00000386966.4:p.Ala248Gly
ENST00000452276.6:c.743C>G	ENSP00000388671.2:p.Ala248Gly
ENST00000453906.6:c.407-5602C>G	ENSP00000403035.2:n.407-5602C>G
ENST00000520680.2:c.743C>G	ENSP00000428785.2:p.Ala248Gly
ENST00000521065.2:c.*460C>G	ENSP00000427947.2:n.*460C>G
ENST00000521517.6:c.743C>G	ENSP00000430740.2:p.Ala248Gly
ENST00000681998.1:c.673C>G	ENSP00000506773.1:n.673C>G
ENST00000682036.1:c.407-5602C>G	ENSP00000508390.1:n.407-5602C>G
ENST00000682577.1:c.673C>G	ENSP00000506963.1:n.673C>G
ENST00000682624.1:c.*317C>G	ENSP00000508343.1:n.*317C>G
ENST00000682700.1:c.743C>G	ENSP00000507627.1:p.Ala248Gly
ENST00000682744.1:n.281C>G
ENST00000682804.1:n.566C>G
ENST00000682837.1:c.498C>G	ENSP00000507920.1:p.Ser166Arg
ENST00000682935.1:n.2303C>G
ENST00000682984.1:c.404C>G	ENSP00000507209.1:p.Ala135Gly
ENST00000683078.1:c.498C>G	ENSP00000506796.1:p.Ser166Arg
ENST00000683223.1:c.584C>G	ENSP00000507685.1:n.584C>G
ENST00000683238.1:n.2124C>G
ENST00000683249.1:n.2324C>G
ENST00000683336.1:c.673C>G	ENSP00000507695.1:n.673C>G
ENST00000683362.1:c.404C>G	ENSP00000506985.1:p.Ala135Gly
ENST00000683850.1:n.666C>G
ENST00000683919.1:c.673C>G	ENSP00000507617.1:n.673C>G
ENST00000683953.1:c.654C>G	ENSP00000508375.1:n.654C>G
ENST00000684023.1:c.877C>G	ENSP00000507461.1:n.877C>G
ENST00000684064.1:c.434C>G	ENSP00000508192.1:p.Ala145Gly
ENST00000684089.1:n.2293C>G
ENST00000684149.1:c.*79C>G	ENSP00000507943.1:n.*79C>G
ENST00000684416.1:n.702C>G
ENST00000684540.1:c.673C>G	ENSP00000507987.1:n.673C>G
ENST00000453321.8:c.743C>G MANE Select	ENSP00000389998.3:p.Ala248Gly
ENST00000323130.7:c.713C>G	ENSP00000314488.3:p.Ala238Gly
ENST00000409623.7:c.500C>G	ENSP00000386966.3:p.Ala167Gly
ENST00000425545.2:n.190C>G
ENST00000452276.5:c.434C>G	ENSP00000388671.1:p.Ala145Gly
ENST00000453321.7:c.743C>G	ENSP00000389998.3:p.Ala248Gly
ENST00000453906.5:c.407-5602C>G	ENSP00000403035.1:n.407-5602C>G
ENST00000474944.5:n.427-5602C>G
ENST00000496213.5:n.208C>G
NM_001142301.1:c.500C>G , LRG_688t2:c.500C>G	NP_001135773.1:p.Ala167Gly
NM_153704.5:c.743C>G , LRG_688t1:c.743C>G	NP_714915.3:p.Ala248Gly
NR_024522.1:n.814C>G
XM_006716686.2:c.440C>G	XP_006716749.1:p.Ala147Gly
XM_006716687.2:c.143C>G	XP_006716750.1:p.Ala48Gly
XM_011517363.1:c.407-5602C>G	XP_011515665.1:n.407-5602C>G
XR_428387.1:n.801C>G
XR_928360.1:n.801C>G
XR_928361.1:n.801C>G
XR_928362.1:n.801C>G
XM_006716686.4:c.440C>G	XP_006716749.1:p.Ala147Gly
XM_011517363.3:c.407-5602C>G	XP_011515665.1:n.407-5602C>G
XM_024447326.1:c.89C>G	XP_024303094.1:p.Ala30Gly
XR_001745619.2:n.784C>G
XR_428387.2:n.784C>G
XR_928360.3:n.784C>G
XR_928362.3:n.784C>G
NM_153704.6:c.743C>G MANE Select	NP_714915.3:p.Ala248Gly
NR_024522.2:n.764C>G