Canonical Allele Identifier: CA1321145902

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957755847
• gnomAD v4: 2-201626057-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626062del , CM000664.2:g.201626062del	GRCh38
NC_000002.11:g.202490785del , CM000664.1:g.202490785del	GRCh37
NC_000002.10:g.202199030del	NCBI36
NG_032049.1:g.22472del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.923del
ENST00000621467.5:c.1001del	ENSP00000480508.2:p.Leu334CysfsTer13
ENST00000686475.1:n.1067del
ENST00000409883.7:c.1127del MANE Select	ENSP00000386264.2:p.Leu376CysfsTer13
ENST00000286196.9:c.*691del	ENSP00000286196.5:n.*691del
ENST00000409444.6:c.1103del	ENSP00000387203.2:p.Leu368CysfsTer13
ENST00000409883.6:c.1127del	ENSP00000386264.2:p.Leu376CysfsTer13
ENST00000471318.5:n.355del
ENST00000495329.1:n.266del
ENST00000621467.4:c.1103del	ENSP00000480508.1:p.Leu368CysfsTer13
NM_001044385.2:c.1127del	NP_001037850.1:p.Leu376CysfsTer13
NM_152388.3:c.1103del	NP_689601.2:p.Leu368CysfsTer13
NM_001044385.3:c.1127del MANE Select	NP_001037850.1:p.Leu376CysfsTer13
NM_152388.4:c.1103del	NP_689601.2:p.Leu368CysfsTer13