Canonical Allele Identifier: CA1321140657

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640296A= , CM000664.2:g.201640296A=	GRCh38
NC_000002.11:g.202505019A= , CM000664.1:g.202505019A=	GRCh37
NC_000002.10:g.202213264A=	NCBI36
NG_032049.1:g.8234T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+597T=	ENSP00000480508.2:n.-356+597T=
ENST00000409883.7:c.75-31T= MANE Select	ENSP00000386264.2:n.75-31T=
ENST00000286196.9:c.-1+597T=	ENSP00000286196.5:n.-1+597T=
ENST00000409444.6:c.51-31T=	ENSP00000387203.2:n.51-31T=
ENST00000409883.6:c.75-31T=	ENSP00000386264.2:n.75-31T=
ENST00000432684.6:c.75-31T=	ENSP00000413230.2:n.75-31T=
ENST00000444047.6:c.75-31T=	ENSP00000402681.2:n.75-31T=
ENST00000463205.2:n.78-31T=
ENST00000489550.5:n.92+597T=
ENST00000621467.4:c.50+597T=	ENSP00000480508.1:n.50+597T=
NM_001044385.2:c.75-31T=	NP_001037850.1:n.75-31T=
NM_152388.3:c.51-31T=	NP_689601.2:n.51-31T=
NM_001044385.3:c.75-31T= MANE Select	NP_001037850.1:n.75-31T=
NM_152388.4:c.51-31T=	NP_689601.2:n.51-31T=