Canonical Allele Identifier: CA461859106

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94798557T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93786329T>G , CM000670.2:g.93786329T>G	GRCh38
NC_000008.10:g.94798557T>G , CM000670.1:g.94798557T>G	GRCh37
NC_000008.9:g.94867733T>G	NCBI36
NG_009190.1:g.36486T>G , LRG_688:g.36486T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.1395T>G	ENSP00000314488.4:p.Ala465=
ENST00000409623.8:c.1350T>G	ENSP00000386966.4:p.Ala450=
ENST00000452276.6:c.1395T>G	ENSP00000388671.2:p.Ala465=
ENST00000453906.6:c.513T>G	ENSP00000403035.2:p.Ala171=
ENST00000520680.2:c.1395T>G	ENSP00000428785.2:p.Ala465=
ENST00000521517.6:c.1395T>G	ENSP00000430740.2:p.Ala465=
ENST00000681998.1:c.1216T>G	ENSP00000506773.1:n.1216T>G
ENST00000682036.1:c.513T>G	ENSP00000508390.1:p.Ala171=
ENST00000682577.1:c.1168T>G	ENSP00000506963.1:n.1168T>G
ENST00000682624.1:c.*969T>G	ENSP00000508343.1:n.*969T>G
ENST00000682700.1:c.1395T>G	ENSP00000507627.1:p.Ala465=
ENST00000682744.1:n.933T>G
ENST00000682804.1:n.1218T>G
ENST00000682837.1:c.884T>G	ENSP00000507920.1:n.884T>G
ENST00000682935.1:n.3445T>G
ENST00000682984.1:c.1056T>G	ENSP00000507209.1:p.Ala352=
ENST00000683078.1:c.1150T>G	ENSP00000506796.1:n.1150T>G
ENST00000683223.1:c.1127T>G	ENSP00000507685.1:n.1127T>G
ENST00000683238.1:n.2619T>G
ENST00000683249.1:n.2992T>G
ENST00000683336.1:c.1216T>G	ENSP00000507695.1:n.1216T>G
ENST00000683362.1:c.1056T>G	ENSP00000506985.1:p.Ala352=
ENST00000683850.1:n.1318T>G
ENST00000683919.1:c.1325T>G	ENSP00000507617.1:n.1325T>G
ENST00000683953.1:c.1306T>G	ENSP00000508375.1:n.1306T>G
ENST00000684023.1:c.1372T>G	ENSP00000507461.1:n.1372T>G
ENST00000684064.1:c.1086T>G	ENSP00000508192.1:p.Ala362=
ENST00000684089.1:n.2945T>G
ENST00000684149.1:c.*574T>G	ENSP00000507943.1:n.*574T>G
ENST00000684416.1:n.1354T>G
ENST00000684540.1:c.1325T>G	ENSP00000507987.1:n.1325T>G
ENST00000453321.8:c.1395T>G MANE Select	ENSP00000389998.3:p.Ala465=
ENST00000323130.7:c.1365T>G	ENSP00000314488.3:p.Ala455=
ENST00000409623.7:c.1152T>G	ENSP00000386966.3:p.Ala384=
ENST00000452276.5:c.1086T>G	ENSP00000388671.1:p.Ala362=
ENST00000453321.7:c.1395T>G	ENSP00000389998.3:p.Ala465=
ENST00000453906.5:c.513T>G	ENSP00000403035.1:p.Ala171=
ENST00000474944.5:n.533T>G
ENST00000520680.1:c.217T>G
NM_001142301.1:c.1152T>G , LRG_688t2:c.1152T>G	NP_001135773.1:p.Ala384=
NM_153704.5:c.1395T>G , LRG_688t1:c.1395T>G	NP_714915.3:p.Ala465=
NR_024522.1:n.1466T>G
XM_006716686.2:c.1092T>G	XP_006716749.1:p.Ala364=
XM_006716687.2:c.795T>G	XP_006716750.1:p.Ala265=
XM_011517363.1:c.513T>G	XP_011515665.1:p.Ala171=
XR_428387.1:n.1453T>G
XR_928360.1:n.1453T>G
XR_928361.1:n.1453T>G
XR_928362.1:n.1453T>G
XM_006716686.4:c.1092T>G	XP_006716749.1:p.Ala364=
XM_011517363.3:c.513T>G	XP_011515665.1:p.Ala171=
XM_024447326.1:c.741T>G	XP_024303094.1:p.Ala247=
XR_001745619.2:n.1436T>G
XR_428387.2:n.1436T>G
XR_928360.3:n.1436T>G
XR_928362.3:n.1436T>G
NM_153704.6:c.1395T>G MANE Select	NP_714915.3:p.Ala465=
NR_024522.2:n.1416T>G