Canonical Allele Identifier: CA1321145921

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626072T= , CM000664.2:g.201626072T=	GRCh38
NC_000002.11:g.202490795T= , CM000664.1:g.202490795T=	GRCh37
NC_000002.10:g.202199040T=	NCBI36
NG_032049.1:g.22458A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.909A=
ENST00000621467.5:c.987A=	ENSP00000480508.2:p.Leu329=
ENST00000686475.1:n.1053A=
ENST00000409883.7:c.1113A= MANE Select	ENSP00000386264.2:p.Leu371=
ENST00000286196.9:c.*677A=	ENSP00000286196.5:n.*677A=
ENST00000409444.6:c.1089A=	ENSP00000387203.2:p.Leu363=
ENST00000409883.6:c.1113A=	ENSP00000386264.2:p.Leu371=
ENST00000471318.5:n.341A=
ENST00000495329.1:n.252A=
ENST00000621467.4:c.1089A=	ENSP00000480508.1:p.Leu363=
NM_001044385.2:c.1113A=	NP_001037850.1:p.Leu371=
NM_152388.3:c.1089A=	NP_689601.2:p.Leu363=
NM_001044385.3:c.1113A= MANE Select	NP_001037850.1:p.Leu371=
NM_152388.4:c.1089A=	NP_689601.2:p.Leu363=