Canonical Allele Identifier: CA461855662

Gene: TMEM67

Linked Data

• gnomAD v4: 8-93780625-T-C
• MyVariant Identifiers: chr8:g.94792853T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780625T>C , CM000670.2:g.93780625T>C	GRCh38
NC_000008.10:g.94792853T>C , CM000670.1:g.94792853T>C	GRCh37
NC_000008.9:g.94862029T>C	NCBI36
NG_009190.1:g.30782T>C , LRG_688:g.30782T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.747T>C	ENSP00000314488.4:p.Leu249=
ENST00000409623.8:c.747T>C	ENSP00000386966.4:p.Leu249=
ENST00000452276.6:c.747T>C	ENSP00000388671.2:p.Leu249=
ENST00000453906.6:c.407-5598T>C	ENSP00000403035.2:n.407-5598T>C
ENST00000520680.2:c.747T>C	ENSP00000428785.2:p.Leu249=
ENST00000521065.2:c.*464T>C	ENSP00000427947.2:n.*464T>C
ENST00000521517.6:c.747T>C	ENSP00000430740.2:p.Leu249=
ENST00000681998.1:c.677T>C	ENSP00000506773.1:n.677T>C
ENST00000682036.1:c.407-5598T>C	ENSP00000508390.1:n.407-5598T>C
ENST00000682577.1:c.677T>C	ENSP00000506963.1:n.677T>C
ENST00000682624.1:c.*321T>C	ENSP00000508343.1:n.*321T>C
ENST00000682700.1:c.747T>C	ENSP00000507627.1:p.Leu249=
ENST00000682744.1:n.285T>C
ENST00000682804.1:n.570T>C
ENST00000682837.1:c.502T>C	ENSP00000507920.1:p.Trp168Arg
ENST00000682935.1:n.2307T>C
ENST00000682984.1:c.408T>C	ENSP00000507209.1:p.Leu136=
ENST00000683078.1:c.502T>C	ENSP00000506796.1:p.Trp168Arg
ENST00000683223.1:c.588T>C	ENSP00000507685.1:n.588T>C
ENST00000683238.1:n.2128T>C
ENST00000683249.1:n.2328T>C
ENST00000683336.1:c.677T>C	ENSP00000507695.1:n.677T>C
ENST00000683362.1:c.408T>C	ENSP00000506985.1:p.Leu136=
ENST00000683850.1:n.670T>C
ENST00000683919.1:c.677T>C	ENSP00000507617.1:n.677T>C
ENST00000683953.1:c.658T>C	ENSP00000508375.1:n.658T>C
ENST00000684023.1:c.881T>C	ENSP00000507461.1:n.881T>C
ENST00000684064.1:c.438T>C	ENSP00000508192.1:p.Leu146=
ENST00000684089.1:n.2297T>C
ENST00000684149.1:c.*83T>C	ENSP00000507943.1:n.*83T>C
ENST00000684416.1:n.706T>C
ENST00000684540.1:c.677T>C	ENSP00000507987.1:n.677T>C
ENST00000453321.8:c.747T>C MANE Select	ENSP00000389998.3:p.Leu249=
ENST00000323130.7:c.717T>C	ENSP00000314488.3:p.Leu239=
ENST00000409623.7:c.504T>C	ENSP00000386966.3:p.Leu168=
ENST00000425545.2:n.194T>C
ENST00000452276.5:c.438T>C	ENSP00000388671.1:p.Leu146=
ENST00000453321.7:c.747T>C	ENSP00000389998.3:p.Leu249=
ENST00000453906.5:c.407-5598T>C	ENSP00000403035.1:n.407-5598T>C
ENST00000474944.5:n.427-5598T>C
ENST00000496213.5:n.212T>C
NM_001142301.1:c.504T>C , LRG_688t2:c.504T>C	NP_001135773.1:p.Leu168=
NM_153704.5:c.747T>C , LRG_688t1:c.747T>C	NP_714915.3:p.Leu249=
NR_024522.1:n.818T>C
XM_006716686.2:c.444T>C	XP_006716749.1:p.Leu148=
XM_006716687.2:c.147T>C	XP_006716750.1:p.Leu49=
XM_011517363.1:c.407-5598T>C	XP_011515665.1:n.407-5598T>C
XR_428387.1:n.805T>C
XR_928360.1:n.805T>C
XR_928361.1:n.805T>C
XR_928362.1:n.805T>C
XM_006716686.4:c.444T>C	XP_006716749.1:p.Leu148=
XM_011517363.3:c.407-5598T>C	XP_011515665.1:n.407-5598T>C
XM_024447326.1:c.93T>C	XP_024303094.1:p.Leu31=
XR_001745619.2:n.788T>C
XR_428387.2:n.788T>C
XR_928360.3:n.788T>C
XR_928362.3:n.788T>C
NM_153704.6:c.747T>C MANE Select	NP_714915.3:p.Leu249=
NR_024522.2:n.768T>C