Canonical Allele Identifier: CA1321146020

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626104C= , CM000664.2:g.201626104C=	GRCh38
NC_000002.11:g.202490827C= , CM000664.1:g.202490827C=	GRCh37
NC_000002.10:g.202199072C=	NCBI36
NG_032049.1:g.22426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.877G=
ENST00000621467.5:c.955G=	ENSP00000480508.2:p.Val319=
ENST00000686475.1:n.1021G=
ENST00000409883.7:c.1081G= MANE Select	ENSP00000386264.2:p.Val361=
ENST00000286196.9:c.*645G=	ENSP00000286196.5:n.*645G=
ENST00000409444.6:c.1057G=	ENSP00000387203.2:p.Val353=
ENST00000409883.6:c.1081G=	ENSP00000386264.2:p.Val361=
ENST00000471318.5:n.309G=
ENST00000495329.1:n.220G=
ENST00000621467.4:c.1057G=	ENSP00000480508.1:p.Val353=
NM_001044385.2:c.1081G=	NP_001037850.1:p.Val361=
NM_152388.3:c.1057G=	NP_689601.2:p.Val353=
NM_001044385.3:c.1081G= MANE Select	NP_001037850.1:p.Val361=
NM_152388.4:c.1057G=	NP_689601.2:p.Val353=