Canonical Allele Identifier: CA10588978

Gene: TMEM231

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75541466A>G , CM000678.2:g.75541466A>G	GRCh38
NC_000016.9:g.75575364A>G , CM000678.1:g.75575364A>G	GRCh37
NC_000016.8:g.74132865A>G	NCBI36
NG_033109.1:g.19821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685935.1:c.*513+1089T>C	ENSP00000510128.1:n.*513+1089T>C
ENST00000686547.1:c.*626-11T>C	ENSP00000508790.1:n.*626-11T>C
ENST00000686680.1:c.350-11T>C	ENSP00000508892.1:n.350-11T>C
ENST00000688195.1:c.293-11T>C	ENSP00000510115.1:n.293-11T>C
ENST00000688270.1:c.676-11T>C	ENSP00000509823.1:n.676-11T>C
ENST00000688618.1:c.*492-11T>C	ENSP00000509271.1:n.*492-11T>C
ENST00000689040.1:c.*763-11T>C	ENSP00000508573.1:n.*763-11T>C
ENST00000692097.1:c.*416-11T>C	ENSP00000509668.1:n.*416-11T>C
ENST00000692689.1:c.317-11T>C	ENSP00000509732.1:n.317-11T>C
ENST00000693457.1:c.*514-810T>C	ENSP00000508414.1:n.*514-810T>C
ENST00000693682.1:c.665-810T>C	ENSP00000508670.1:n.665-810T>C
ENST00000258173.11:c.665-11T>C MANE Select	ENSP00000258173.5:n.665-11T>C
ENST00000258173.10:c.665-11T>C	ENSP00000258173.5:n.665-11T>C
ENST00000460606.1:c.159+1136T>C
ENST00000562410.5:c.*467-11T>C	ENSP00000454582.1:n.*467-11T>C
ENST00000564318.1:n.579T>C
ENST00000564576.1:n.475-11T>C
ENST00000565067.5:c.521-11T>C	ENSP00000457254.1:n.521-11T>C
ENST00000568377.5:c.752-11T>C	ENSP00000476267.1:n.752-11T>C
ENST00000569294.1:n.409-11T>C
ENST00000570006.5:c.*45-11T>C	ENSP00000455520.1:n.*45-11T>C
NM_001077416.2:c.824-11T>C	NP_001070884.2:n.824-11T>C
NM_001077418.2:c.665-11T>C	NP_001070886.1:n.665-11T>C
NR_074083.1:n.865-11T>C
NM_001077418.3:c.665-11T>C MANE Select	NP_001070886.1:n.665-11T>C
NR_074083.2:n.831-11T>C