Canonical Allele Identifier: CA1321146190

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626293T= , CM000664.2:g.201626293T=	GRCh38
NC_000002.11:g.202491016T= , CM000664.1:g.202491016T=	GRCh37
NC_000002.10:g.202199261T=	NCBI36
NG_032049.1:g.22237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-146A=
ENST00000621467.5:c.912-146A=	ENSP00000480508.2:n.912-146A=
ENST00000686475.1:n.978-146A=
ENST00000409883.7:c.1038-146A= MANE Select	ENSP00000386264.2:n.1038-146A=
ENST00000286196.9:c.*602-146A=	ENSP00000286196.5:n.*602-146A=
ENST00000409444.6:c.1014-146A=	ENSP00000387203.2:n.1014-146A=
ENST00000409883.6:c.1038-146A=	ENSP00000386264.2:n.1038-146A=
ENST00000471318.5:n.266-146A=
ENST00000495329.1:n.31A=
ENST00000621467.4:c.1014-146A=	ENSP00000480508.1:n.1014-146A=
NM_001044385.2:c.1038-146A=	NP_001037850.1:n.1038-146A=
NM_152388.3:c.1014-146A=	NP_689601.2:n.1014-146A=
NM_001044385.3:c.1038-146A= MANE Select	NP_001037850.1:n.1038-146A=
NM_152388.4:c.1014-146A=	NP_689601.2:n.1014-146A=