Canonical Allele Identifier: CA371688371

Gene: TMEM67

Linked Data

• COSMIC: COSM1102484 ; COSM1597854
• MyVariant Identifiers: chr8:g.94793161T>C (hg19) ; chr8:g.93780933T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780933T>C , CM000670.2:g.93780933T>C	GRCh38
NC_000008.10:g.94793161T>C , CM000670.1:g.94793161T>C	GRCh37
NC_000008.9:g.94862337T>C	NCBI36
NG_009190.1:g.31090T>C , LRG_688:g.31090T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.929T>C	ENSP00000314488.4:p.Leu310Pro
ENST00000409623.8:c.929T>C	ENSP00000386966.4:p.Leu310Pro
ENST00000452276.6:c.929T>C	ENSP00000388671.2:p.Leu310Pro
ENST00000453906.6:c.407-5290T>C	ENSP00000403035.2:n.407-5290T>C
ENST00000520680.2:c.929T>C	ENSP00000428785.2:p.Leu310Pro
ENST00000521065.2:c.*646T>C	ENSP00000427947.2:n.*646T>C
ENST00000521517.6:c.929T>C	ENSP00000430740.2:p.Leu310Pro
ENST00000681998.1:c.799+186T>C	ENSP00000506773.1:n.799+186T>C
ENST00000682036.1:c.407-5290T>C	ENSP00000508390.1:n.407-5290T>C
ENST00000682577.1:c.859T>C	ENSP00000506963.1:n.859T>C
ENST00000682624.1:c.*503T>C	ENSP00000508343.1:n.*503T>C
ENST00000682700.1:c.929T>C	ENSP00000507627.1:p.Leu310Pro
ENST00000682744.1:n.467T>C
ENST00000682804.1:n.752T>C
ENST00000682837.1:c.624+186T>C	ENSP00000507920.1:n.624+186T>C
ENST00000682935.1:n.2489T>C
ENST00000682984.1:c.590T>C	ENSP00000507209.1:p.Leu197Pro
ENST00000683078.1:c.684T>C	ENSP00000506796.1:n.684T>C
ENST00000683223.1:c.710+186T>C	ENSP00000507685.1:n.710+186T>C
ENST00000683238.1:n.2310T>C
ENST00000683249.1:n.2526T>C
ENST00000683336.1:c.799+186T>C	ENSP00000507695.1:n.799+186T>C
ENST00000683362.1:c.590T>C	ENSP00000506985.1:p.Leu197Pro
ENST00000683850.1:n.852T>C
ENST00000683919.1:c.859T>C	ENSP00000507617.1:n.859T>C
ENST00000683953.1:c.840T>C	ENSP00000508375.1:n.840T>C
ENST00000684023.1:c.1063T>C	ENSP00000507461.1:n.1063T>C
ENST00000684064.1:c.620T>C	ENSP00000508192.1:p.Leu207Pro
ENST00000684089.1:n.2479T>C
ENST00000684149.1:c.*265T>C	ENSP00000507943.1:n.*265T>C
ENST00000684416.1:n.888T>C
ENST00000684540.1:c.859T>C	ENSP00000507987.1:n.859T>C
ENST00000453321.8:c.929T>C MANE Select	ENSP00000389998.3:p.Leu310Pro
ENST00000323130.7:c.899T>C	ENSP00000314488.3:p.Leu300Pro
ENST00000409623.7:c.686T>C	ENSP00000386966.3:p.Leu229Pro
ENST00000425545.2:n.376T>C
ENST00000452276.5:c.620T>C	ENSP00000388671.1:p.Leu207Pro
ENST00000453321.7:c.929T>C	ENSP00000389998.3:p.Leu310Pro
ENST00000453906.5:c.407-5290T>C	ENSP00000403035.1:n.407-5290T>C
ENST00000474944.5:n.427-5290T>C
ENST00000496213.5:n.394T>C
NM_001142301.1:c.686T>C , LRG_688t2:c.686T>C	NP_001135773.1:p.Leu229Pro
NM_153704.5:c.929T>C , LRG_688t1:c.929T>C	NP_714915.3:p.Leu310Pro
NR_024522.1:n.1000T>C
XM_006716686.2:c.626T>C	XP_006716749.1:p.Leu209Pro
XM_006716687.2:c.329T>C	XP_006716750.1:p.Leu110Pro
XM_011517363.1:c.407-5290T>C	XP_011515665.1:n.407-5290T>C
XR_428387.1:n.987T>C
XR_928360.1:n.987T>C
XR_928361.1:n.987T>C
XR_928362.1:n.987T>C
XM_006716686.4:c.626T>C	XP_006716749.1:p.Leu209Pro
XM_011517363.3:c.407-5290T>C	XP_011515665.1:n.407-5290T>C
XM_024447326.1:c.275T>C	XP_024303094.1:p.Leu92Pro
XR_001745619.2:n.970T>C
XR_428387.2:n.970T>C
XR_928360.3:n.970T>C
XR_928362.3:n.970T>C
NM_153704.6:c.929T>C MANE Select	NP_714915.3:p.Leu310Pro
NR_024522.2:n.950T>C