Canonical Allele Identifier: CA1321145884

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626050T= , CM000664.2:g.201626050T=	GRCh38
NC_000002.11:g.202490773T= , CM000664.1:g.202490773T=	GRCh37
NC_000002.10:g.202199018T=	NCBI36
NG_032049.1:g.22480A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.931A=
ENST00000621467.5:c.1009A=	ENSP00000480508.2:p.Arg337=
ENST00000686475.1:n.1075A=
ENST00000409883.7:c.1135A= MANE Select	ENSP00000386264.2:p.Arg379=
ENST00000286196.9:c.*699A=	ENSP00000286196.5:n.*699A=
ENST00000409444.6:c.1111A=	ENSP00000387203.2:p.Arg371=
ENST00000409883.6:c.1135A=	ENSP00000386264.2:p.Arg379=
ENST00000471318.5:n.363A=
ENST00000495329.1:n.274A=
ENST00000621467.4:c.1111A=	ENSP00000480508.1:p.Arg371=
NM_001044385.2:c.1135A=	NP_001037850.1:p.Arg379=
NM_152388.3:c.1111A=	NP_689601.2:p.Arg371=
NM_001044385.3:c.1135A= MANE Select	NP_001037850.1:p.Arg379=
NM_152388.4:c.1111A=	NP_689601.2:p.Arg371=