Canonical Allele Identifier: CA371687854

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94792894C>A (hg19) ; chr8:g.93780666C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780666C>A , CM000670.2:g.93780666C>A	GRCh38
NC_000008.10:g.94792894C>A , CM000670.1:g.94792894C>A	GRCh37
NC_000008.9:g.94862070C>A	NCBI36
NG_009190.1:g.30823C>A , LRG_688:g.30823C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.788C>A	ENSP00000314488.4:p.Ala263Asp
ENST00000409623.8:c.788C>A	ENSP00000386966.4:p.Ala263Asp
ENST00000452276.6:c.788C>A	ENSP00000388671.2:p.Ala263Asp
ENST00000453906.6:c.407-5557C>A	ENSP00000403035.2:n.407-5557C>A
ENST00000520680.2:c.788C>A	ENSP00000428785.2:p.Ala263Asp
ENST00000521065.2:c.*505C>A	ENSP00000427947.2:n.*505C>A
ENST00000521517.6:c.788C>A	ENSP00000430740.2:p.Ala263Asp
ENST00000681998.1:c.718C>A	ENSP00000506773.1:n.718C>A
ENST00000682036.1:c.407-5557C>A	ENSP00000508390.1:n.407-5557C>A
ENST00000682577.1:c.718C>A	ENSP00000506963.1:n.718C>A
ENST00000682624.1:c.*362C>A	ENSP00000508343.1:n.*362C>A
ENST00000682700.1:c.788C>A	ENSP00000507627.1:p.Ala263Asp
ENST00000682744.1:n.326C>A
ENST00000682804.1:n.611C>A
ENST00000682837.1:c.543C>A	ENSP00000507920.1:p.Cys181Ter
ENST00000682935.1:n.2348C>A
ENST00000682984.1:c.449C>A	ENSP00000507209.1:p.Ala150Asp
ENST00000683078.1:c.543C>A	ENSP00000506796.1:p.Cys181Ter
ENST00000683223.1:c.629C>A	ENSP00000507685.1:n.629C>A
ENST00000683238.1:n.2169C>A
ENST00000683249.1:n.2369C>A
ENST00000683336.1:c.718C>A	ENSP00000507695.1:n.718C>A
ENST00000683362.1:c.449C>A	ENSP00000506985.1:p.Ala150Asp
ENST00000683850.1:n.711C>A
ENST00000683919.1:c.718C>A	ENSP00000507617.1:n.718C>A
ENST00000683953.1:c.699C>A	ENSP00000508375.1:n.699C>A
ENST00000684023.1:c.922C>A	ENSP00000507461.1:n.922C>A
ENST00000684064.1:c.479C>A	ENSP00000508192.1:p.Ala160Asp
ENST00000684089.1:n.2338C>A
ENST00000684149.1:c.*124C>A	ENSP00000507943.1:n.*124C>A
ENST00000684416.1:n.747C>A
ENST00000684540.1:c.718C>A	ENSP00000507987.1:n.718C>A
ENST00000453321.8:c.788C>A MANE Select	ENSP00000389998.3:p.Ala263Asp
ENST00000323130.7:c.758C>A	ENSP00000314488.3:p.Ala253Asp
ENST00000409623.7:c.545C>A	ENSP00000386966.3:p.Ala182Asp
ENST00000425545.2:n.235C>A
ENST00000452276.5:c.479C>A	ENSP00000388671.1:p.Ala160Asp
ENST00000453321.7:c.788C>A	ENSP00000389998.3:p.Ala263Asp
ENST00000453906.5:c.407-5557C>A	ENSP00000403035.1:n.407-5557C>A
ENST00000474944.5:n.427-5557C>A
ENST00000496213.5:n.253C>A
NM_001142301.1:c.545C>A , LRG_688t2:c.545C>A	NP_001135773.1:p.Ala182Asp
NM_153704.5:c.788C>A , LRG_688t1:c.788C>A	NP_714915.3:p.Ala263Asp
NR_024522.1:n.859C>A
XM_006716686.2:c.485C>A	XP_006716749.1:p.Ala162Asp
XM_006716687.2:c.188C>A	XP_006716750.1:p.Ala63Asp
XM_011517363.1:c.407-5557C>A	XP_011515665.1:n.407-5557C>A
XR_428387.1:n.846C>A
XR_928360.1:n.846C>A
XR_928361.1:n.846C>A
XR_928362.1:n.846C>A
XM_006716686.4:c.485C>A	XP_006716749.1:p.Ala162Asp
XM_011517363.3:c.407-5557C>A	XP_011515665.1:n.407-5557C>A
XM_024447326.1:c.134C>A	XP_024303094.1:p.Ala45Asp
XR_001745619.2:n.829C>A
XR_428387.2:n.829C>A
XR_928360.3:n.829C>A
XR_928362.3:n.829C>A
NM_153704.6:c.788C>A MANE Select	NP_714915.3:p.Ala263Asp
NR_024522.2:n.809C>A