Canonical Allele Identifier: CA1321145977

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626095C= , CM000664.2:g.201626095C=	GRCh38
NC_000002.11:g.202490818C= , CM000664.1:g.202490818C=	GRCh37
NC_000002.10:g.202199063C=	NCBI36
NG_032049.1:g.22435G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.886G=
ENST00000621467.5:c.964G=	ENSP00000480508.2:p.Val322=
ENST00000686475.1:n.1030G=
ENST00000409883.7:c.1090G= MANE Select	ENSP00000386264.2:p.Val364=
ENST00000286196.9:c.*654G=	ENSP00000286196.5:n.*654G=
ENST00000409444.6:c.1066G=	ENSP00000387203.2:p.Val356=
ENST00000409883.6:c.1090G=	ENSP00000386264.2:p.Val364=
ENST00000471318.5:n.318G=
ENST00000495329.1:n.229G=
ENST00000621467.4:c.1066G=	ENSP00000480508.1:p.Val356=
NM_001044385.2:c.1090G=	NP_001037850.1:p.Val364=
NM_152388.3:c.1066G=	NP_689601.2:p.Val356=
NM_001044385.3:c.1090G= MANE Select	NP_001037850.1:p.Val364=
NM_152388.4:c.1066G=	NP_689601.2:p.Val356=