Canonical Allele Identifier: CA350310403

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201629770C>T , CM000664.2:g.201629770C>T	GRCh38
NC_000002.11:g.202494493C>T , CM000664.1:g.202494493C>T	GRCh37
NC_000002.10:g.202202738C>T	NCBI36
NG_032049.1:g.18760G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.636G>A MANE Select	NP_001037850.1:p.Trp212Ter
ENST00000409883.7:c.636G>A MANE Select	ENSP00000386264.2:p.Trp212Ter
NM_001044385.2:c.636G>A	NP_001037850.1:p.Trp212Ter
NM_152388.3:c.612G>A	NP_689601.2:p.Trp204Ter
NM_152388.4:c.612G>A	NP_689601.2:p.Trp204Ter
ENST00000286196.9:c.*200G>A	ENSP00000286196.5:n.*200G>A
ENST00000409444.6:c.612G>A	ENSP00000387203.2:p.Trp204Ter
ENST00000409883.6:c.636G>A	ENSP00000386264.2:p.Trp212Ter
ENST00000432684.6:c.*435G>A	ENSP00000413230.2:n.*435G>A
ENST00000444047.6:c.*446G>A	ENSP00000402681.2:n.*446G>A
ENST00000466641.5:n.334G>A
ENST00000466839.5:n.504G>A
ENST00000471318.6:n.526G>A
ENST00000621467.4:c.612G>A	ENSP00000480508.1:p.Trp204Ter
ENST00000621467.5:c.510G>A	ENSP00000480508.2:p.Trp170Ter
ENST00000686475.1:n.576G>A