Canonical Allele Identifier: CA1321145995

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626096G= , CM000664.2:g.201626096G=	GRCh38
NC_000002.11:g.202490819G= , CM000664.1:g.202490819G=	GRCh37
NC_000002.10:g.202199064G=	NCBI36
NG_032049.1:g.22434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.885C=
ENST00000621467.5:c.963C=	ENSP00000480508.2:p.Leu321=
ENST00000686475.1:n.1029C=
ENST00000409883.7:c.1089C= MANE Select	ENSP00000386264.2:p.Leu363=
ENST00000286196.9:c.*653C=	ENSP00000286196.5:n.*653C=
ENST00000409444.6:c.1065C=	ENSP00000387203.2:p.Leu355=
ENST00000409883.6:c.1089C=	ENSP00000386264.2:p.Leu363=
ENST00000471318.5:n.317C=
ENST00000495329.1:n.228C=
ENST00000621467.4:c.1065C=	ENSP00000480508.1:p.Leu355=
NM_001044385.2:c.1089C=	NP_001037850.1:p.Leu363=
NM_152388.3:c.1065C=	NP_689601.2:p.Leu355=
NM_001044385.3:c.1089C= MANE Select	NP_001037850.1:p.Leu363=
NM_152388.4:c.1065C=	NP_689601.2:p.Leu355=