Canonical Allele Identifier: CA2577211815

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626064del , CM000664.2:g.201626064del	GRCh38
NC_000002.11:g.202490787del , CM000664.1:g.202490787del	GRCh37
NC_000002.10:g.202199032del	NCBI36
NG_032049.1:g.22466del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.917del
ENST00000621467.5:c.995del	ENSP00000480508.2:p.Leu332HisfsTer15
ENST00000686475.1:n.1061del
ENST00000409883.7:c.1121del MANE Select	ENSP00000386264.2:p.Leu374HisfsTer15
ENST00000286196.9:c.*685del	ENSP00000286196.5:n.*685del
ENST00000409444.6:c.1097del	ENSP00000387203.2:p.Leu366HisfsTer15
ENST00000409883.6:c.1121del	ENSP00000386264.2:p.Leu374HisfsTer15
ENST00000471318.5:n.349del
ENST00000495329.1:n.260del
ENST00000621467.4:c.1097del	ENSP00000480508.1:p.Leu366HisfsTer15
NM_001044385.2:c.1121del	NP_001037850.1:p.Leu374HisfsTer15
NM_152388.3:c.1097del	NP_689601.2:p.Leu366HisfsTer15
NM_001044385.3:c.1121del MANE Select	NP_001037850.1:p.Leu374HisfsTer15
NM_152388.4:c.1097del	NP_689601.2:p.Leu366HisfsTer15