Canonical Allele Identifier: CA2056361

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201628129G>C , CM000664.2:g.201628129G>C	GRCh38
NC_000002.11:g.202492852G>C , CM000664.1:g.202492852G>C	GRCh37
NC_000002.10:g.202201097G>C	NCBI36
NG_032049.1:g.20401C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.890C>G MANE Select	NP_001037850.1:p.Ser297Ter
ENST00000409883.7:c.890C>G MANE Select	ENSP00000386264.2:p.Ser297Ter
NM_001044385.2:c.890C>G	NP_001037850.1:p.Ser297Ter
NM_152388.3:c.866C>G	NP_689601.2:p.Ser289Ter
NM_152388.4:c.866C>G	NP_689601.2:p.Ser289Ter
ENST00000286196.9:c.*454C>G	ENSP00000286196.5:n.*454C>G
ENST00000409444.6:c.866C>G	ENSP00000387203.2:p.Ser289Ter
ENST00000409883.6:c.890C>G	ENSP00000386264.2:p.Ser297Ter
ENST00000466641.5:n.588C>G
ENST00000466839.5:n.758C>G
ENST00000471318.5:n.212C>G
ENST00000471318.6:n.780C>G
ENST00000621467.4:c.866C>G	ENSP00000480508.1:p.Ser289Ter
ENST00000621467.5:c.764C>G	ENSP00000480508.2:p.Ser255Ter
ENST00000686475.1:n.830C>G