Canonical Allele Identifier: CA2056397

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201629321T>C , CM000664.2:g.201629321T>C	GRCh38
NC_000002.11:g.202494044T>C , CM000664.1:g.202494044T>C	GRCh37
NC_000002.10:g.202202289T>C	NCBI36
NG_032049.1:g.19209A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.778A>G MANE Select	NP_001037850.1:p.Asn260Asp
ENST00000409883.7:c.778A>G MANE Select	ENSP00000386264.2:p.Asn260Asp
NM_001044385.2:c.778A>G	NP_001037850.1:p.Asn260Asp
NM_152388.3:c.754A>G	NP_689601.2:p.Asn252Asp
NM_152388.4:c.754A>G	NP_689601.2:p.Asn252Asp
ENST00000286196.9:c.*342A>G	ENSP00000286196.5:n.*342A>G
ENST00000409444.6:c.754A>G	ENSP00000387203.2:p.Asn252Asp
ENST00000409883.6:c.778A>G	ENSP00000386264.2:p.Asn260Asp
ENST00000432684.6:c.*577A>G	ENSP00000413230.2:n.*577A>G
ENST00000466641.5:n.476A>G
ENST00000466839.5:n.646A>G
ENST00000471318.5:n.100A>G
ENST00000471318.6:n.668A>G
ENST00000621467.4:c.754A>G	ENSP00000480508.1:p.Asn252Asp
ENST00000621467.5:c.652A>G	ENSP00000480508.2:p.Asn218Asp
ENST00000686475.1:n.718A>G