Canonical Allele Identifier: CA396804611

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75542601C>T , CM000678.2:g.75542601C>T	GRCh38
NC_000016.9:g.75576499C>T , CM000678.1:g.75576499C>T	GRCh37
NC_000016.8:g.74134000C>T	NCBI36
NG_033109.1:g.18686G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001077418.3:c.664+1G>A MANE Select	NP_001070886.1:n.664+1G>A
ENST00000258173.11:c.664+1G>A MANE Select	ENSP00000258173.5:n.664+1G>A
NM_001077416.2:c.823+1G>A	NP_001070884.2:n.823+1G>A
NM_001077418.2:c.664+1G>A	NP_001070886.1:n.664+1G>A
NR_074083.1:n.864+1G>A
NR_074083.2:n.830+1G>A
ENST00000258173.10:c.664+1G>A	ENSP00000258173.5:n.664+1G>A
ENST00000460606.1:c.159+1G>A
ENST00000562410.5:c.*466+1G>A	ENSP00000454582.1:n.*466+1G>A
ENST00000564576.1:n.428G>A
ENST00000565067.5:c.520+1G>A	ENSP00000457254.1:n.520+1G>A
ENST00000568377.5:c.751+1G>A	ENSP00000476267.1:n.751+1G>A
ENST00000569294.1:n.408+1G>A
ENST00000570006.5:c.*44+1G>A	ENSP00000455520.1:n.*44+1G>A
ENST00000685935.1:c.*467G>A	ENSP00000510128.1:n.*467G>A
ENST00000686547.1:c.*625+1G>A	ENSP00000508790.1:n.*625+1G>A
ENST00000686680.1:c.349+1G>A	ENSP00000508892.1:n.349+1G>A
ENST00000688195.1:c.292+1G>A	ENSP00000510115.1:n.292+1G>A
ENST00000688270.1:c.665G>A	ENSP00000509823.1:p.Gly222Asp
ENST00000688618.1:c.*466+1G>A	ENSP00000509271.1:n.*466+1G>A
ENST00000689040.1:c.*762+1G>A	ENSP00000508573.1:n.*762+1G>A
ENST00000692097.1:c.*415+1G>A	ENSP00000509668.1:n.*415+1G>A
ENST00000692689.1:c.316+1G>A	ENSP00000509732.1:n.316+1G>A
ENST00000693457.1:c.*467G>A	ENSP00000508414.1:n.*467G>A
ENST00000693682.1:c.664+1G>A	ENSP00000508670.1:n.664+1G>A