Canonical Allele Identifier: CA2056471

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201632129T>C , CM000664.2:g.201632129T>C	GRCh38
NC_000002.11:g.202496852T>C , CM000664.1:g.202496852T>C	GRCh37
NC_000002.10:g.202205097T>C	NCBI36
NG_032049.1:g.16401A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.475A>G MANE Select	NP_001037850.1:p.Thr159Ala
ENST00000409883.7:c.475A>G MANE Select	ENSP00000386264.2:p.Thr159Ala
NM_001044385.2:c.475A>G	NP_001037850.1:p.Thr159Ala
NM_152388.3:c.451A>G	NP_689601.2:p.Thr151Ala
NM_152388.4:c.451A>G	NP_689601.2:p.Thr151Ala
ENST00000286196.9:c.*39A>G	ENSP00000286196.5:n.*39A>G
ENST00000409444.6:c.451A>G	ENSP00000387203.2:p.Thr151Ala
ENST00000409883.6:c.475A>G	ENSP00000386264.2:p.Thr159Ala
ENST00000432684.6:c.*274A>G	ENSP00000413230.2:n.*274A>G
ENST00000444047.6:c.*285A>G	ENSP00000402681.2:n.*285A>G
ENST00000466641.5:n.173A>G
ENST00000471318.6:n.365A>G
ENST00000621467.4:c.451A>G	ENSP00000480508.1:p.Thr151Ala
ENST00000621467.5:c.349A>G	ENSP00000480508.2:p.Thr117Ala
ENST00000686475.1:n.415A>G