Canonical Allele Identifier: CA2056517

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201633381G>A , CM000664.2:g.201633381G>A	GRCh38
NC_000002.11:g.202498104G>A , CM000664.1:g.202498104G>A	GRCh37
NC_000002.10:g.202206349G>A	NCBI36
NG_032049.1:g.15149C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.325C>T MANE Select	NP_001037850.1:p.Arg109Ter
ENST00000409883.7:c.325C>T MANE Select	ENSP00000386264.2:p.Arg109Ter
NM_001044385.2:c.325C>T	NP_001037850.1:p.Arg109Ter
NM_152388.3:c.301C>T	NP_689601.2:p.Arg101Ter
NM_152388.4:c.301C>T	NP_689601.2:p.Arg101Ter
ENST00000286196.9:c.246C>T	ENSP00000286196.5:p.Tyr82=
ENST00000409444.6:c.301C>T	ENSP00000387203.2:p.Arg101Ter
ENST00000409883.6:c.325C>T	ENSP00000386264.2:p.Arg109Ter
ENST00000432684.6:c.*124C>T	ENSP00000413230.2:n.*124C>T
ENST00000444047.6:c.*135C>T	ENSP00000402681.2:n.*135C>T
ENST00000466641.5:n.23C>T
ENST00000471318.6:n.215C>T
ENST00000489550.5:n.428C>T
ENST00000621467.4:c.301C>T	ENSP00000480508.1:p.Arg101Ter
ENST00000621467.5:c.199C>T	ENSP00000480508.2:p.Arg67Ter
ENST00000686475.1:n.161C>T