Canonical Allele Identifier: CA2056357

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201628118G>A , CM000664.2:g.201628118G>A	GRCh38
NC_000002.11:g.202492841G>A , CM000664.1:g.202492841G>A	GRCh37
NC_000002.10:g.202201086G>A	NCBI36
NG_032049.1:g.20412C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.901C>T MANE Select	NP_001037850.1:p.Arg301Ter
ENST00000409883.7:c.901C>T MANE Select	ENSP00000386264.2:p.Arg301Ter
NM_001044385.2:c.901C>T	NP_001037850.1:p.Arg301Ter
NM_152388.3:c.877C>T	NP_689601.2:p.Arg293Ter
NM_152388.4:c.877C>T	NP_689601.2:p.Arg293Ter
ENST00000286196.9:c.*465C>T	ENSP00000286196.5:n.*465C>T
ENST00000409444.6:c.877C>T	ENSP00000387203.2:p.Arg293Ter
ENST00000409883.6:c.901C>T	ENSP00000386264.2:p.Arg301Ter
ENST00000466641.5:n.599C>T
ENST00000466839.5:n.769C>T
ENST00000471318.5:n.223C>T
ENST00000471318.6:n.791C>T
ENST00000621467.4:c.877C>T	ENSP00000480508.1:p.Arg293Ter
ENST00000621467.5:c.775C>T	ENSP00000480508.2:p.Arg259Ter
ENST00000686475.1:n.841C>T