Canonical Allele Identifier: CA2056554

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201636846C>T , CM000664.2:g.201636846C>T	GRCh38
NC_000002.11:g.202501569C>T , CM000664.1:g.202501569C>T	GRCh37
NC_000002.10:g.202209814C>T	NCBI36
NG_032049.1:g.11684G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.176G>A MANE Select	NP_001037850.1:p.Arg59Gln
ENST00000409883.7:c.176G>A MANE Select	ENSP00000386264.2:p.Arg59Gln
NM_001044385.2:c.176G>A	NP_001037850.1:p.Arg59Gln
NM_152388.3:c.152G>A	NP_689601.2:p.Arg51Gln
NM_152388.4:c.152G>A	NP_689601.2:p.Arg51Gln
ENST00000286196.9:c.97G>A	ENSP00000286196.5:p.Glu33Lys
ENST00000409444.6:c.152G>A	ENSP00000387203.2:p.Arg51Gln
ENST00000409883.6:c.176G>A	ENSP00000386264.2:p.Arg59Gln
ENST00000432684.6:c.176G>A	ENSP00000413230.2:p.Arg59Gln
ENST00000444047.6:c.176G>A	ENSP00000402681.2:p.Arg59Gln
ENST00000471318.6:n.66G>A
ENST00000480124.1:n.83G>A
ENST00000489550.5:n.189G>A
ENST00000621467.4:c.152G>A	ENSP00000480508.1:p.Arg51Gln
ENST00000621467.5:c.50G>A	ENSP00000480508.2:p.Arg17Gln
ENST00000686475.1:n.12G>A