Canonical Allele Identifier: CA371687821

Gene: TMEM67

Linked Data

• MyVariant Identifiers: chr8:g.94792880T>G (hg19) ; chr8:g.93780652T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93780652T>G , CM000670.2:g.93780652T>G	GRCh38
NC_000008.10:g.94792880T>G , CM000670.1:g.94792880T>G	GRCh37
NC_000008.9:g.94862056T>G	NCBI36
NG_009190.1:g.30809T>G , LRG_688:g.30809T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323130.8:c.774T>G	ENSP00000314488.4:p.Asn258Lys
ENST00000409623.8:c.774T>G	ENSP00000386966.4:p.Asn258Lys
ENST00000452276.6:c.774T>G	ENSP00000388671.2:p.Asn258Lys
ENST00000453906.6:c.407-5571T>G	ENSP00000403035.2:n.407-5571T>G
ENST00000520680.2:c.774T>G	ENSP00000428785.2:p.Asn258Lys
ENST00000521065.2:c.*491T>G	ENSP00000427947.2:n.*491T>G
ENST00000521517.6:c.774T>G	ENSP00000430740.2:p.Asn258Lys
ENST00000681998.1:c.704T>G	ENSP00000506773.1:n.704T>G
ENST00000682036.1:c.407-5571T>G	ENSP00000508390.1:n.407-5571T>G
ENST00000682577.1:c.704T>G	ENSP00000506963.1:n.704T>G
ENST00000682624.1:c.*348T>G	ENSP00000508343.1:n.*348T>G
ENST00000682700.1:c.774T>G	ENSP00000507627.1:p.Asn258Lys
ENST00000682744.1:n.312T>G
ENST00000682804.1:n.597T>G
ENST00000682837.1:c.529T>G	ENSP00000507920.1:p.Phe177Val
ENST00000682935.1:n.2334T>G
ENST00000682984.1:c.435T>G	ENSP00000507209.1:p.Asn145Lys
ENST00000683078.1:c.529T>G	ENSP00000506796.1:p.Phe177Val
ENST00000683223.1:c.615T>G	ENSP00000507685.1:n.615T>G
ENST00000683238.1:n.2155T>G
ENST00000683249.1:n.2355T>G
ENST00000683336.1:c.704T>G	ENSP00000507695.1:n.704T>G
ENST00000683362.1:c.435T>G	ENSP00000506985.1:p.Asn145Lys
ENST00000683850.1:n.697T>G
ENST00000683919.1:c.704T>G	ENSP00000507617.1:n.704T>G
ENST00000683953.1:c.685T>G	ENSP00000508375.1:n.685T>G
ENST00000684023.1:c.908T>G	ENSP00000507461.1:n.908T>G
ENST00000684064.1:c.465T>G	ENSP00000508192.1:p.Asn155Lys
ENST00000684089.1:n.2324T>G
ENST00000684149.1:c.*110T>G	ENSP00000507943.1:n.*110T>G
ENST00000684416.1:n.733T>G
ENST00000684540.1:c.704T>G	ENSP00000507987.1:n.704T>G
ENST00000453321.8:c.774T>G MANE Select	ENSP00000389998.3:p.Asn258Lys
ENST00000323130.7:c.744T>G	ENSP00000314488.3:p.Asn248Lys
ENST00000409623.7:c.531T>G	ENSP00000386966.3:p.Asn177Lys
ENST00000425545.2:n.221T>G
ENST00000452276.5:c.465T>G	ENSP00000388671.1:p.Asn155Lys
ENST00000453321.7:c.774T>G	ENSP00000389998.3:p.Asn258Lys
ENST00000453906.5:c.407-5571T>G	ENSP00000403035.1:n.407-5571T>G
ENST00000474944.5:n.427-5571T>G
ENST00000496213.5:n.239T>G
NM_001142301.1:c.531T>G , LRG_688t2:c.531T>G	NP_001135773.1:p.Asn177Lys
NM_153704.5:c.774T>G , LRG_688t1:c.774T>G	NP_714915.3:p.Asn258Lys
NR_024522.1:n.845T>G
XM_006716686.2:c.471T>G	XP_006716749.1:p.Asn157Lys
XM_006716687.2:c.174T>G	XP_006716750.1:p.Asn58Lys
XM_011517363.1:c.407-5571T>G	XP_011515665.1:n.407-5571T>G
XR_428387.1:n.832T>G
XR_928360.1:n.832T>G
XR_928361.1:n.832T>G
XR_928362.1:n.832T>G
XM_006716686.4:c.471T>G	XP_006716749.1:p.Asn157Lys
XM_011517363.3:c.407-5571T>G	XP_011515665.1:n.407-5571T>G
XM_024447326.1:c.120T>G	XP_024303094.1:p.Asn40Lys
XR_001745619.2:n.815T>G
XR_428387.2:n.815T>G
XR_928360.3:n.815T>G
XR_928362.3:n.815T>G
NM_153704.6:c.774T>G MANE Select	NP_714915.3:p.Asn258Lys
NR_024522.2:n.795T>G