Canonical Allele Identifier: CA181326420

Gene: TMEM67

Linked Data

• ClinVar Variation Id: 1651748
• ClinVar RCV Id: RCV002154136 ; RCV002494480
• dbSNP Id: rs966581270
• gnomAD v2: 8-94792886-C-T
• gnomAD v3: 8-93780658-C-T
• gnomAD v4: 8-93780658-C-T
• COSMIC: COSM3651820 ; COSM3651821 ; COSM3651822
• MyVariant Identifiers: chr8:g.94792886C>T (hg19) ; chr8:g.93780658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780658C>T , CM000670.2:g.93780658C>T	GRCh38
NC_000008.10:g.94792886C>T , CM000670.1:g.94792886C>T	GRCh37
NC_000008.9:g.94862062C>T	NCBI36
NG_009190.1:g.30815C>T , LRG_688:g.30815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.780C>T	ENSP00000314488.4:p.Tyr260=
ENST00000409623.8:c.780C>T	ENSP00000386966.4:p.Tyr260=
ENST00000452276.6:c.780C>T	ENSP00000388671.2:p.Tyr260=
ENST00000453906.6:c.407-5565C>T	ENSP00000403035.2:n.407-5565C>T
ENST00000520680.2:c.780C>T	ENSP00000428785.2:p.Tyr260=
ENST00000521065.2:c.*497C>T	ENSP00000427947.2:n.*497C>T
ENST00000521517.6:c.780C>T	ENSP00000430740.2:p.Tyr260=
ENST00000681998.1:c.710C>T	ENSP00000506773.1:n.710C>T
ENST00000682036.1:c.407-5565C>T	ENSP00000508390.1:n.407-5565C>T
ENST00000682577.1:c.710C>T	ENSP00000506963.1:n.710C>T
ENST00000682624.1:c.*354C>T	ENSP00000508343.1:n.*354C>T
ENST00000682700.1:c.780C>T	ENSP00000507627.1:p.Tyr260=
ENST00000682744.1:n.318C>T
ENST00000682804.1:n.603C>T
ENST00000682837.1:c.535C>T	ENSP00000507920.1:p.Arg179Ter
ENST00000682935.1:n.2340C>T
ENST00000682984.1:c.441C>T	ENSP00000507209.1:p.Tyr147=
ENST00000683078.1:c.535C>T	ENSP00000506796.1:p.Arg179Ter
ENST00000683223.1:c.621C>T	ENSP00000507685.1:n.621C>T
ENST00000683238.1:n.2161C>T
ENST00000683249.1:n.2361C>T
ENST00000683336.1:c.710C>T	ENSP00000507695.1:n.710C>T
ENST00000683362.1:c.441C>T	ENSP00000506985.1:p.Tyr147=
ENST00000683850.1:n.703C>T
ENST00000683919.1:c.710C>T	ENSP00000507617.1:n.710C>T
ENST00000683953.1:c.691C>T	ENSP00000508375.1:n.691C>T
ENST00000684023.1:c.914C>T	ENSP00000507461.1:n.914C>T
ENST00000684064.1:c.471C>T	ENSP00000508192.1:p.Tyr157=
ENST00000684089.1:n.2330C>T
ENST00000684149.1:c.*116C>T	ENSP00000507943.1:n.*116C>T
ENST00000684416.1:n.739C>T
ENST00000684540.1:c.710C>T	ENSP00000507987.1:n.710C>T
ENST00000453321.8:c.780C>T MANE Select	ENSP00000389998.3:p.Tyr260=
ENST00000323130.7:c.750C>T	ENSP00000314488.3:p.Tyr250=
ENST00000409623.7:c.537C>T	ENSP00000386966.3:p.Tyr179=
ENST00000425545.2:n.227C>T
ENST00000452276.5:c.471C>T	ENSP00000388671.1:p.Tyr157=
ENST00000453321.7:c.780C>T	ENSP00000389998.3:p.Tyr260=
ENST00000453906.5:c.407-5565C>T	ENSP00000403035.1:n.407-5565C>T
ENST00000474944.5:n.427-5565C>T
ENST00000496213.5:n.245C>T
NM_001142301.1:c.537C>T , LRG_688t2:c.537C>T	NP_001135773.1:p.Tyr179=
NM_153704.5:c.780C>T , LRG_688t1:c.780C>T	NP_714915.3:p.Tyr260=
NR_024522.1:n.851C>T
XM_006716686.2:c.477C>T	XP_006716749.1:p.Tyr159=
XM_006716687.2:c.180C>T	XP_006716750.1:p.Tyr60=
XM_011517363.1:c.407-5565C>T	XP_011515665.1:n.407-5565C>T
XR_428387.1:n.838C>T
XR_928360.1:n.838C>T
XR_928361.1:n.838C>T
XR_928362.1:n.838C>T
XM_006716686.4:c.477C>T	XP_006716749.1:p.Tyr159=
XM_011517363.3:c.407-5565C>T	XP_011515665.1:n.407-5565C>T
XM_024447326.1:c.126C>T	XP_024303094.1:p.Tyr42=
XR_001745619.2:n.821C>T
XR_428387.2:n.821C>T
XR_928360.3:n.821C>T
XR_928362.3:n.821C>T
NM_153704.6:c.780C>T MANE Select	NP_714915.3:p.Tyr260=
NR_024522.2:n.801C>T