Canonical Allele Identifier: CA63955656

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201632186G>A , CM000664.2:g.201632186G>A	GRCh38
NC_000002.11:g.202496909G>A , CM000664.1:g.202496909G>A	GRCh37
NC_000002.10:g.202205154G>A	NCBI36
NG_032049.1:g.16344C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.418C>T MANE Select	NP_001037850.1:p.Gln140Ter
ENST00000409883.7:c.418C>T MANE Select	ENSP00000386264.2:p.Gln140Ter
NM_001044385.2:c.418C>T	NP_001037850.1:p.Gln140Ter
NM_152388.3:c.394C>T	NP_689601.2:p.Gln132Ter
NM_152388.4:c.394C>T	NP_689601.2:p.Gln132Ter
ENST00000286196.9:c.339C>T	ENSP00000286196.5:p.Tyr113=
ENST00000409444.6:c.394C>T	ENSP00000387203.2:p.Gln132Ter
ENST00000409883.6:c.418C>T	ENSP00000386264.2:p.Gln140Ter
ENST00000432684.6:c.*217C>T	ENSP00000413230.2:n.*217C>T
ENST00000444047.6:c.*228C>T	ENSP00000402681.2:n.*228C>T
ENST00000466641.5:n.116C>T
ENST00000471318.6:n.308C>T
ENST00000489550.5:n.521C>T
ENST00000621467.4:c.394C>T	ENSP00000480508.1:p.Gln132Ter
ENST00000621467.5:c.292C>T	ENSP00000480508.2:p.Gln98Ter
ENST00000686475.1:n.358C>T