Canonical Allele Identifier: CA1321140606

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640264G= , CM000664.2:g.201640264G=	GRCh38
NC_000002.11:g.202504987G= , CM000664.1:g.202504987G=	GRCh37
NC_000002.10:g.202213232G=	NCBI36
NG_032049.1:g.8266C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.-356+629C=	ENSP00000480508.2:n.-356+629C=
ENST00000409883.7:c.76C= MANE Select	ENSP00000386264.2:p.Gln26=
ENST00000286196.9:c.-1+629C=	ENSP00000286196.5:n.-1+629C=
ENST00000409444.6:c.52C=	ENSP00000387203.2:p.Gln18=
ENST00000409883.6:c.76C=	ENSP00000386264.2:p.Gln26=
ENST00000432684.6:c.76C=	ENSP00000413230.2:p.Gln26=
ENST00000444047.6:c.76C=	ENSP00000402681.2:p.Gln26=
ENST00000463205.2:n.79C=
ENST00000489550.5:n.92+629C=
ENST00000621467.4:c.50+629C=	ENSP00000480508.1:n.50+629C=
NM_001044385.2:c.76C=	NP_001037850.1:p.Gln26=
NM_152388.3:c.52C=	NP_689601.2:p.Gln18=
NM_001044385.3:c.76C= MANE Select	NP_001037850.1:p.Gln26=
NM_152388.4:c.52C=	NP_689601.2:p.Gln18=