Canonical Allele Identifier: CA396810580

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75556177G>T , CM000678.2:g.75556177G>T	GRCh38
NC_000016.9:g.75590075G>T , CM000678.1:g.75590075G>T	GRCh37
NC_000016.8:g.74147576G>T	NCBI36
NG_033109.1:g.5110C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001077418.3:c.33C>A MANE Select	NP_001070886.1:p.Val11=
ENST00000258173.11:c.33C>A MANE Select	ENSP00000258173.5:p.Val11=
NM_001077416.2:c.95C>A	NP_001070884.2:p.Ser32Ter
NM_001077418.2:c.33C>A	NP_001070886.1:p.Val11=
NR_074083.1:n.110C>A
NR_074083.2:n.76C>A
ENST00000258173.10:c.33C>A	ENSP00000258173.5:p.Val11=
ENST00000561809.1:n.86C>A
ENST00000562410.5:c.33C>A	ENSP00000454582.1:p.Val11=
ENST00000564576.1:n.69C>A
ENST00000565067.5:c.33C>A	ENSP00000457254.1:p.Val11=
ENST00000568377.5:c.23C>A	ENSP00000476267.1:p.Ser8Ter
ENST00000570006.5:c.33C>A	ENSP00000455520.1:p.Val11=
ENST00000685935.1:c.33C>A	ENSP00000510128.1:p.Val11=
ENST00000686547.1:c.33C>A	ENSP00000508790.1:p.Val11=
ENST00000688270.1:c.33C>A	ENSP00000509823.1:p.Val11=
ENST00000688618.1:c.33C>A	ENSP00000509271.1:p.Val11=
ENST00000689040.1:c.33C>A	ENSP00000508573.1:p.Val11=
ENST00000692097.1:c.33C>A	ENSP00000509668.1:p.Val11=
ENST00000692215.1:n.76C>A
ENST00000693457.1:c.33C>A	ENSP00000508414.1:p.Val11=
ENST00000693682.1:c.33C>A	ENSP00000508670.1:p.Val11=