Canonical Allele Identifier: CA350316296

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201639047T>C , CM000664.2:g.201639047T>C	GRCh38
NC_000002.11:g.202503770T>C , CM000664.1:g.202503770T>C	GRCh37
NC_000002.10:g.202212015T>C	NCBI36
NG_032049.1:g.9483A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.80-2A>G MANE Select	NP_001037850.1:n.80-2A>G
ENST00000409883.7:c.80-2A>G MANE Select	ENSP00000386264.2:n.80-2A>G
NM_001044385.2:c.80-2A>G	NP_001037850.1:n.80-2A>G
NM_152388.3:c.56-2A>G	NP_689601.2:n.56-2A>G
NM_152388.4:c.56-2A>G	NP_689601.2:n.56-2A>G
ENST00000286196.9:c.1-2A>G	ENSP00000286196.5:n.1-2A>G
ENST00000409444.6:c.56-2A>G	ENSP00000387203.2:n.56-2A>G
ENST00000409883.6:c.80-2A>G	ENSP00000386264.2:n.80-2A>G
ENST00000432684.6:c.80-2A>G	ENSP00000413230.2:n.80-2A>G
ENST00000444047.6:c.80-2A>G	ENSP00000402681.2:n.80-2A>G
ENST00000463205.2:n.83-2A>G
ENST00000489550.5:n.93-2A>G
ENST00000621467.4:c.54A>G	ENSP00000480508.1:p.Ile18Met
ENST00000621467.5:c.-355-2A>G	ENSP00000480508.2:n.-355-2A>G