Canonical Allele Identifier: CA63958480

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201636847G>A , CM000664.2:g.201636847G>A	GRCh38
NC_000002.11:g.202501570G>A , CM000664.1:g.202501570G>A	GRCh37
NC_000002.10:g.202209815G>A	NCBI36
NG_032049.1:g.11683C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.175C>T MANE Select	NP_001037850.1:p.Arg59Ter
ENST00000409883.7:c.175C>T MANE Select	ENSP00000386264.2:p.Arg59Ter
NM_001044385.2:c.175C>T	NP_001037850.1:p.Arg59Ter
NM_152388.3:c.151C>T	NP_689601.2:p.Arg51Ter
NM_152388.4:c.151C>T	NP_689601.2:p.Arg51Ter
ENST00000286196.9:c.96C>T	ENSP00000286196.5:p.Val32=
ENST00000409444.6:c.151C>T	ENSP00000387203.2:p.Arg51Ter
ENST00000409883.6:c.175C>T	ENSP00000386264.2:p.Arg59Ter
ENST00000432684.6:c.175C>T	ENSP00000413230.2:p.Arg59Ter
ENST00000444047.6:c.175C>T	ENSP00000402681.2:p.Arg59Ter
ENST00000471318.6:n.65C>T
ENST00000480124.1:n.82C>T
ENST00000489550.5:n.188C>T
ENST00000621467.4:c.151C>T	ENSP00000480508.1:p.Arg51Ter
ENST00000621467.5:c.49C>T	ENSP00000480508.2:p.Arg17Ter
ENST00000686475.1:n.11C>T