Canonical Allele Identifier: CA350312990

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201632117G>A , CM000664.2:g.201632117G>A	GRCh38
NC_000002.11:g.202496840G>A , CM000664.1:g.202496840G>A	GRCh37
NC_000002.10:g.202205085G>A	NCBI36
NG_032049.1:g.16413C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.487C>T MANE Select	NP_001037850.1:p.Gln163Ter
ENST00000409883.7:c.487C>T MANE Select	ENSP00000386264.2:p.Gln163Ter
NM_001044385.2:c.487C>T	NP_001037850.1:p.Gln163Ter
NM_152388.3:c.463C>T	NP_689601.2:p.Gln155Ter
NM_152388.4:c.463C>T	NP_689601.2:p.Gln155Ter
ENST00000286196.9:c.*51C>T	ENSP00000286196.5:n.*51C>T
ENST00000409444.6:c.463C>T	ENSP00000387203.2:p.Gln155Ter
ENST00000409883.6:c.487C>T	ENSP00000386264.2:p.Gln163Ter
ENST00000432684.6:c.*286C>T	ENSP00000413230.2:n.*286C>T
ENST00000444047.6:c.*297C>T	ENSP00000402681.2:n.*297C>T
ENST00000466641.5:n.185C>T
ENST00000471318.6:n.377C>T
ENST00000621467.4:c.463C>T	ENSP00000480508.1:p.Gln155Ter
ENST00000621467.5:c.361C>T	ENSP00000480508.2:p.Gln121Ter
ENST00000686475.1:n.427C>T