Canonical Allele Identifier: CA396806690

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75545399G>A , CM000678.2:g.75545399G>A	GRCh38
NC_000016.9:g.75579297G>A , CM000678.1:g.75579297G>A	GRCh37
NC_000016.8:g.74136798G>A	NCBI36
NG_033109.1:g.15888C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001077418.3:c.535C>T MANE Select	NP_001070886.1:p.Gln179Ter
ENST00000258173.11:c.535C>T MANE Select	ENSP00000258173.5:p.Gln179Ter
NM_001077416.2:c.694C>T	NP_001070884.2:p.Gln232Ter
NM_001077418.2:c.535C>T	NP_001070886.1:p.Gln179Ter
NR_074083.1:n.735C>T
NR_074083.2:n.701C>T
ENST00000258173.10:c.535C>T	ENSP00000258173.5:p.Gln179Ter
ENST00000460606.1:c.30C>T
ENST00000562410.5:c.*337C>T	ENSP00000454582.1:n.*337C>T
ENST00000564576.1:n.346-2716C>T
ENST00000565067.5:c.438+427C>T	ENSP00000457254.1:n.438+427C>T
ENST00000568377.5:c.622C>T	ENSP00000476267.1:p.Gln208Ter
ENST00000569294.1:n.279C>T
ENST00000570006.5:c.497C>T	ENSP00000455520.1:p.Ala166Val
ENST00000685935.1:c.*337C>T	ENSP00000510128.1:n.*337C>T
ENST00000686547.1:c.*496C>T	ENSP00000508790.1:n.*496C>T
ENST00000686680.1:c.220C>T	ENSP00000508892.1:p.Gln74Ter
ENST00000688195.1:c.163C>T	ENSP00000510115.1:p.Gln55Ter
ENST00000688270.1:c.535C>T	ENSP00000509823.1:p.Gln179Ter
ENST00000688618.1:c.*337C>T	ENSP00000509271.1:n.*337C>T
ENST00000689040.1:c.*337C>T	ENSP00000508573.1:n.*337C>T
ENST00000692097.1:c.*286C>T	ENSP00000509668.1:n.*286C>T
ENST00000692689.1:c.187C>T	ENSP00000509732.1:p.Gln63Ter
ENST00000693457.1:c.*337C>T	ENSP00000508414.1:n.*337C>T
ENST00000693682.1:c.535C>T	ENSP00000508670.1:p.Gln179Ter