Canonical Allele Identifier: CA1321145911

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626070G= , CM000664.2:g.201626070G=	GRCh38
NC_000002.11:g.202490793G= , CM000664.1:g.202490793G=	GRCh37
NC_000002.10:g.202199038G=	NCBI36
NG_032049.1:g.22460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.911C=
ENST00000621467.5:c.989C=	ENSP00000480508.2:p.Ser330=
ENST00000686475.1:n.1055C=
ENST00000409883.7:c.1115C= MANE Select	ENSP00000386264.2:p.Ser372=
ENST00000286196.9:c.*679C=	ENSP00000286196.5:n.*679C=
ENST00000409444.6:c.1091C=	ENSP00000387203.2:p.Ser364=
ENST00000409883.6:c.1115C=	ENSP00000386264.2:p.Ser372=
ENST00000471318.5:n.343C=
ENST00000495329.1:n.254C=
ENST00000621467.4:c.1091C=	ENSP00000480508.1:p.Ser364=
NM_001044385.2:c.1115C=	NP_001037850.1:p.Ser372=
NM_152388.3:c.1091C=	NP_689601.2:p.Ser364=
NM_001044385.3:c.1115C= MANE Select	NP_001037850.1:p.Ser372=
NM_152388.4:c.1091C=	NP_689601.2:p.Ser364=