Canonical Allele Identifier: CA2233413700

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75540031G= , CM000678.2:g.75540031G=	GRCh38
NC_000016.9:g.75573929G= , CM000678.1:g.75573929G=	GRCh37
NC_000016.8:g.74131430G=	NCBI36
NG_029853.1:g.140C=
NG_033109.1:g.21256C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685935.1:c.*548C=	ENSP00000510128.1:n.*548C=
ENST00000686680.1:c.599C=	ENSP00000508892.1:p.Thr200=
ENST00000688195.1:c.542C=	ENSP00000510115.1:p.Thr181=
ENST00000688270.1:c.*235C=	ENSP00000509823.1:n.*235C=
ENST00000688618.1:c.*741C=	ENSP00000509271.1:n.*741C=
ENST00000689040.1:c.*1021C=	ENSP00000508573.1:n.*1021C=
ENST00000692097.1:c.*665C=	ENSP00000509668.1:n.*665C=
ENST00000692689.1:c.566C=	ENSP00000509732.1:p.Thr189=
ENST00000693457.1:c.*1139C=	ENSP00000508414.1:n.*1139C=
ENST00000693682.1:c.*558C=	ENSP00000508670.1:n.*558C=
ENST00000258173.11:c.914C= MANE Select	ENSP00000258173.5:p.Thr305=
ENST00000258173.10:c.914C=	ENSP00000258173.5:p.Thr305=
ENST00000460606.1:c.159+2571C=
ENST00000562410.5:c.*716C=	ENSP00000454582.1:n.*716C=
ENST00000564318.1:n.839C=
ENST00000565067.5:c.770C=	ENSP00000457254.1:p.Thr257=
ENST00000568377.5:c.1001C=	ENSP00000476267.1:p.Thr334=
ENST00000570006.5:c.*294C=	ENSP00000455520.1:n.*294C=
NM_001077416.2:c.1073C=	NP_001070884.2:p.Thr358=
NM_001077418.2:c.914C=	NP_001070886.1:p.Thr305=
NR_074083.1:n.1114C=
NM_001077418.3:c.914C= MANE Select	NP_001070886.1:p.Thr305=
NR_074083.2:n.1080C=