Canonical Allele Identifier: CA461859036

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94798539A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93786311A>C , CM000670.2:g.93786311A>C	GRCh38
NC_000008.10:g.94798539A>C , CM000670.1:g.94798539A>C	GRCh37
NC_000008.9:g.94867715A>C	NCBI36
NG_009190.1:g.36468A>C , LRG_688:g.36468A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.1377A>C	ENSP00000314488.4:p.Pro459=
ENST00000409623.8:c.1332A>C	ENSP00000386966.4:p.Pro444=
ENST00000452276.6:c.1377A>C	ENSP00000388671.2:p.Pro459=
ENST00000453906.6:c.495A>C	ENSP00000403035.2:p.Pro165=
ENST00000520680.2:c.1377A>C	ENSP00000428785.2:p.Pro459=
ENST00000521517.6:c.1377A>C	ENSP00000430740.2:p.Pro459=
ENST00000681998.1:c.1198A>C	ENSP00000506773.1:n.1198A>C
ENST00000682036.1:c.495A>C	ENSP00000508390.1:p.Pro165=
ENST00000682577.1:c.1150A>C	ENSP00000506963.1:n.1150A>C
ENST00000682624.1:c.*951A>C	ENSP00000508343.1:n.*951A>C
ENST00000682700.1:c.1377A>C	ENSP00000507627.1:p.Pro459=
ENST00000682744.1:n.915A>C
ENST00000682804.1:n.1200A>C
ENST00000682837.1:c.866A>C	ENSP00000507920.1:n.866A>C
ENST00000682935.1:n.3427A>C
ENST00000682984.1:c.1038A>C	ENSP00000507209.1:p.Pro346=
ENST00000683078.1:c.1132A>C	ENSP00000506796.1:n.1132A>C
ENST00000683223.1:c.1109A>C	ENSP00000507685.1:n.1109A>C
ENST00000683238.1:n.2601A>C
ENST00000683249.1:n.2974A>C
ENST00000683336.1:c.1198A>C	ENSP00000507695.1:n.1198A>C
ENST00000683362.1:c.1038A>C	ENSP00000506985.1:p.Pro346=
ENST00000683850.1:n.1300A>C
ENST00000683919.1:c.1307A>C	ENSP00000507617.1:n.1307A>C
ENST00000683953.1:c.1288A>C	ENSP00000508375.1:n.1288A>C
ENST00000684023.1:c.1354A>C	ENSP00000507461.1:n.1354A>C
ENST00000684064.1:c.1068A>C	ENSP00000508192.1:p.Pro356=
ENST00000684089.1:n.2927A>C
ENST00000684149.1:c.*556A>C	ENSP00000507943.1:n.*556A>C
ENST00000684416.1:n.1336A>C
ENST00000684540.1:c.1307A>C	ENSP00000507987.1:n.1307A>C
ENST00000453321.8:c.1377A>C MANE Select	ENSP00000389998.3:p.Pro459=
ENST00000323130.7:c.1347A>C	ENSP00000314488.3:p.Pro449=
ENST00000409623.7:c.1134A>C	ENSP00000386966.3:p.Pro378=
ENST00000452276.5:c.1068A>C	ENSP00000388671.1:p.Pro356=
ENST00000453321.7:c.1377A>C	ENSP00000389998.3:p.Pro459=
ENST00000453906.5:c.495A>C	ENSP00000403035.1:p.Pro165=
ENST00000474944.5:n.515A>C
ENST00000520680.1:c.199A>C
NM_001142301.1:c.1134A>C , LRG_688t2:c.1134A>C	NP_001135773.1:p.Pro378=
NM_153704.5:c.1377A>C , LRG_688t1:c.1377A>C	NP_714915.3:p.Pro459=
NR_024522.1:n.1448A>C
XM_006716686.2:c.1074A>C	XP_006716749.1:p.Pro358=
XM_006716687.2:c.777A>C	XP_006716750.1:p.Pro259=
XM_011517363.1:c.495A>C	XP_011515665.1:p.Pro165=
XR_428387.1:n.1435A>C
XR_928360.1:n.1435A>C
XR_928361.1:n.1435A>C
XR_928362.1:n.1435A>C
XM_006716686.4:c.1074A>C	XP_006716749.1:p.Pro358=
XM_011517363.3:c.495A>C	XP_011515665.1:p.Pro165=
XM_024447326.1:c.723A>C	XP_024303094.1:p.Pro241=
XR_001745619.2:n.1418A>C
XR_428387.2:n.1418A>C
XR_928360.3:n.1418A>C
XR_928362.3:n.1418A>C
NM_153704.6:c.1377A>C MANE Select	NP_714915.3:p.Pro459=
NR_024522.2:n.1398A>C