Canonical Allele Identifier: CA350310049

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201629730T>C , CM000664.2:g.201629730T>C	GRCh38
NC_000002.11:g.202494453T>C , CM000664.1:g.202494453T>C	GRCh37
NC_000002.10:g.202202698T>C	NCBI36
NG_032049.1:g.18800A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.676A>G MANE Select	NP_001037850.1:p.Arg226Gly
ENST00000409883.7:c.676A>G MANE Select	ENSP00000386264.2:p.Arg226Gly
NM_001044385.2:c.676A>G	NP_001037850.1:p.Arg226Gly
NM_152388.3:c.652A>G	NP_689601.2:p.Arg218Gly
NM_152388.4:c.652A>G	NP_689601.2:p.Arg218Gly
ENST00000286196.9:c.*240A>G	ENSP00000286196.5:n.*240A>G
ENST00000409444.6:c.652A>G	ENSP00000387203.2:p.Arg218Gly
ENST00000409883.6:c.676A>G	ENSP00000386264.2:p.Arg226Gly
ENST00000432684.6:c.*475A>G	ENSP00000413230.2:n.*475A>G
ENST00000444047.6:c.*486A>G	ENSP00000402681.2:n.*486A>G
ENST00000466641.5:n.374A>G
ENST00000466839.5:n.544A>G
ENST00000471318.6:n.566A>G
ENST00000621467.4:c.652A>G	ENSP00000480508.1:p.Arg218Gly
ENST00000621467.5:c.550A>G	ENSP00000480508.2:p.Arg184Gly
ENST00000686475.1:n.616A>G