Canonical Allele Identifier: CA2056403

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201629374C>T , CM000664.2:g.201629374C>T	GRCh38
NC_000002.11:g.202494097C>T , CM000664.1:g.202494097C>T	GRCh37
NC_000002.10:g.202202342C>T	NCBI36
NG_032049.1:g.19156G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.725G>A MANE Select	NP_001037850.1:p.Trp242Ter
ENST00000409883.7:c.725G>A MANE Select	ENSP00000386264.2:p.Trp242Ter
NM_001044385.2:c.725G>A	NP_001037850.1:p.Trp242Ter
NM_152388.3:c.701G>A	NP_689601.2:p.Trp234Ter
NM_152388.4:c.701G>A	NP_689601.2:p.Trp234Ter
ENST00000286196.9:c.*289G>A	ENSP00000286196.5:n.*289G>A
ENST00000409444.6:c.701G>A	ENSP00000387203.2:p.Trp234Ter
ENST00000409883.6:c.725G>A	ENSP00000386264.2:p.Trp242Ter
ENST00000432684.6:c.*524G>A	ENSP00000413230.2:n.*524G>A
ENST00000466641.5:n.423G>A
ENST00000466839.5:n.593G>A
ENST00000471318.5:n.47G>A
ENST00000471318.6:n.615G>A
ENST00000621467.4:c.701G>A	ENSP00000480508.1:p.Trp234Ter
ENST00000621467.5:c.599G>A	ENSP00000480508.2:p.Trp200Ter
ENST00000686475.1:n.665G>A