Canonical Allele Identifier: CA396802285

Gene: TMEM231

Linked Data

• MyVariant Identifiers: chr16:g.75573933C>T (hg19) ; chr16:g.75540035C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75540035C>T , CM000678.2:g.75540035C>T	GRCh38
NC_000016.9:g.75573933C>T , CM000678.1:g.75573933C>T	GRCh37
NC_000016.8:g.74131434C>T	NCBI36
NG_029853.1:g.136G>A
NG_033109.1:g.21252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685935.1:c.*544G>A	ENSP00000510128.1:n.*544G>A
ENST00000686680.1:c.595G>A	ENSP00000508892.1:p.Val199Met
ENST00000688195.1:c.538G>A	ENSP00000510115.1:p.Val180Met
ENST00000688270.1:c.*231G>A	ENSP00000509823.1:n.*231G>A
ENST00000688618.1:c.*737G>A	ENSP00000509271.1:n.*737G>A
ENST00000689040.1:c.*1017G>A	ENSP00000508573.1:n.*1017G>A
ENST00000692097.1:c.*661G>A	ENSP00000509668.1:n.*661G>A
ENST00000692689.1:c.562G>A	ENSP00000509732.1:p.Val188Met
ENST00000693457.1:c.*1135G>A	ENSP00000508414.1:n.*1135G>A
ENST00000693682.1:c.*554G>A	ENSP00000508670.1:n.*554G>A
ENST00000258173.11:c.910G>A MANE Select	ENSP00000258173.5:p.Val304Met
ENST00000258173.10:c.910G>A	ENSP00000258173.5:p.Val304Met
ENST00000460606.1:c.159+2567G>A
ENST00000562410.5:c.*712G>A	ENSP00000454582.1:n.*712G>A
ENST00000564318.1:n.835G>A
ENST00000565067.5:c.766G>A	ENSP00000457254.1:p.Val256Met
ENST00000568377.5:c.997G>A	ENSP00000476267.1:p.Val333Met
ENST00000570006.5:c.*290G>A	ENSP00000455520.1:n.*290G>A
NM_001077416.2:c.1069G>A	NP_001070884.2:p.Val357Met
NM_001077418.2:c.910G>A	NP_001070886.1:p.Val304Met
NR_074083.1:n.1110G>A
NM_001077418.3:c.910G>A MANE Select	NP_001070886.1:p.Val304Met
NR_074083.2:n.1076G>A