Canonical Allele Identifier: CA371689692

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94798481G>C (hg19) ; chr8:g.93786253G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93786253G>C , CM000670.2:g.93786253G>C	GRCh38
NC_000008.10:g.94798481G>C , CM000670.1:g.94798481G>C	GRCh37
NC_000008.9:g.94867657G>C	NCBI36
NG_009190.1:g.36410G>C , LRG_688:g.36410G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000323130.8:c.1319G>C	ENSP00000314488.4:p.Arg440Pro
ENST00000409623.8:c.1289-15G>C	ENSP00000386966.4:n.1289-15G>C
ENST00000452276.6:c.1319G>C	ENSP00000388671.2:p.Arg440Pro
ENST00000453906.6:c.437G>C	ENSP00000403035.2:p.Arg146Pro
ENST00000520680.2:c.1319G>C	ENSP00000428785.2:p.Arg440Pro
ENST00000521517.6:c.1319G>C	ENSP00000430740.2:p.Arg440Pro
ENST00000681998.1:c.1140G>C	ENSP00000506773.1:n.1140G>C
ENST00000682036.1:c.437G>C	ENSP00000508390.1:p.Arg146Pro
ENST00000682577.1:c.1092G>C	ENSP00000506963.1:n.1092G>C
ENST00000682624.1:c.*893G>C	ENSP00000508343.1:n.*893G>C
ENST00000682700.1:c.1319G>C	ENSP00000507627.1:p.Arg440Pro
ENST00000682744.1:n.857G>C
ENST00000682804.1:n.1142G>C
ENST00000682837.1:c.808G>C	ENSP00000507920.1:n.808G>C
ENST00000682935.1:n.3369G>C
ENST00000682984.1:c.980G>C	ENSP00000507209.1:p.Arg327Pro
ENST00000683078.1:c.1074G>C	ENSP00000506796.1:n.1074G>C
ENST00000683223.1:c.1051G>C	ENSP00000507685.1:n.1051G>C
ENST00000683238.1:n.2543G>C
ENST00000683249.1:n.2916G>C
ENST00000683336.1:c.1140G>C	ENSP00000507695.1:n.1140G>C
ENST00000683362.1:c.980G>C	ENSP00000506985.1:p.Arg327Pro
ENST00000683850.1:n.1242G>C
ENST00000683919.1:c.1249G>C	ENSP00000507617.1:n.1249G>C
ENST00000683953.1:c.1230G>C	ENSP00000508375.1:n.1230G>C
ENST00000684023.1:c.1296G>C	ENSP00000507461.1:n.1296G>C
ENST00000684064.1:c.1010G>C	ENSP00000508192.1:p.Arg337Pro
ENST00000684089.1:n.2869G>C
ENST00000684149.1:c.*498G>C	ENSP00000507943.1:n.*498G>C
ENST00000684416.1:n.1278G>C
ENST00000684540.1:c.1249G>C	ENSP00000507987.1:n.1249G>C
ENST00000453321.8:c.1319G>C MANE Select	ENSP00000389998.3:p.Arg440Pro
ENST00000323130.7:c.1289G>C	ENSP00000314488.3:p.Arg430Pro
ENST00000409623.7:c.1076G>C	ENSP00000386966.3:p.Arg359Pro
ENST00000452276.5:c.1010G>C	ENSP00000388671.1:p.Arg337Pro
ENST00000453321.7:c.1319G>C	ENSP00000389998.3:p.Arg440Pro
ENST00000453906.5:c.437G>C	ENSP00000403035.1:p.Arg146Pro
ENST00000474944.5:n.457G>C
ENST00000520680.1:c.141G>C
NM_001142301.1:c.1076G>C , LRG_688t2:c.1076G>C	NP_001135773.1:p.Arg359Pro
NM_153704.5:c.1319G>C , LRG_688t1:c.1319G>C	NP_714915.3:p.Arg440Pro
NR_024522.1:n.1390G>C
XM_006716686.2:c.1016G>C	XP_006716749.1:p.Arg339Pro
XM_006716687.2:c.719G>C	XP_006716750.1:p.Arg240Pro
XM_011517363.1:c.437G>C	XP_011515665.1:p.Arg146Pro
XR_428387.1:n.1377G>C
XR_928360.1:n.1377G>C
XR_928361.1:n.1377G>C
XR_928362.1:n.1377G>C
XM_006716686.4:c.1016G>C	XP_006716749.1:p.Arg339Pro
XM_011517363.3:c.437G>C	XP_011515665.1:p.Arg146Pro
XM_024447326.1:c.665G>C	XP_024303094.1:p.Arg222Pro
XR_001745619.2:n.1360G>C
XR_428387.2:n.1360G>C
XR_928360.3:n.1360G>C
XR_928362.3:n.1360G>C
NM_153704.6:c.1319G>C MANE Select	NP_714915.3:p.Arg440Pro
NR_024522.2:n.1340G>C