Canonical Allele Identifier: CA8176191

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75545506T>C , CM000678.2:g.75545506T>C	GRCh38
NC_000016.9:g.75579404T>C , CM000678.1:g.75579404T>C	GRCh37
NC_000016.8:g.74136905T>C	NCBI36
NG_033109.1:g.15781A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001077418.3:c.439-11A>G MANE Select	NP_001070886.1:n.439-11A>G
ENST00000258173.11:c.439-11A>G MANE Select	ENSP00000258173.5:n.439-11A>G
NM_001077416.2:c.598-11A>G	NP_001070884.2:n.598-11A>G
NM_001077418.2:c.439-11A>G	NP_001070886.1:n.439-11A>G
NR_074083.1:n.639-11A>G
NR_074083.2:n.605-11A>G
ENST00000258173.10:c.439-11A>G	ENSP00000258173.5:n.439-11A>G
ENST00000562410.5:c.*241-11A>G	ENSP00000454582.1:n.*241-11A>G
ENST00000564576.1:n.346-2823A>G
ENST00000565067.5:c.438+320A>G	ENSP00000457254.1:n.438+320A>G
ENST00000568377.5:c.526-11A>G	ENSP00000476267.1:n.526-11A>G
ENST00000569294.1:n.183-11A>G
ENST00000570006.5:c.401-11A>G	ENSP00000455520.1:n.401-11A>G
ENST00000685935.1:c.*241-11A>G	ENSP00000510128.1:n.*241-11A>G
ENST00000686547.1:c.*400-11A>G	ENSP00000508790.1:n.*400-11A>G
ENST00000686680.1:c.124-11A>G	ENSP00000508892.1:n.124-11A>G
ENST00000688195.1:c.67-11A>G	ENSP00000510115.1:n.67-11A>G
ENST00000688270.1:c.439-11A>G	ENSP00000509823.1:n.439-11A>G
ENST00000688618.1:c.*241-11A>G	ENSP00000509271.1:n.*241-11A>G
ENST00000689040.1:c.*241-11A>G	ENSP00000508573.1:n.*241-11A>G
ENST00000692097.1:c.*190-11A>G	ENSP00000509668.1:n.*190-11A>G
ENST00000692689.1:c.91-11A>G	ENSP00000509732.1:n.91-11A>G
ENST00000693457.1:c.*241-11A>G	ENSP00000508414.1:n.*241-11A>G
ENST00000693682.1:c.439-11A>G	ENSP00000508670.1:n.439-11A>G