Canonical Allele Identifier: CA2662657576

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626130-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626132del , CM000664.2:g.201626132del	GRCh38
NC_000002.11:g.202490855del , CM000664.1:g.202490855del	GRCh37
NC_000002.10:g.202199100del	NCBI36
NG_032049.1:g.22399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.850del
ENST00000621467.5:c.928del	ENSP00000480508.2:p.Glu310AsnfsTer10
ENST00000686475.1:n.994del
ENST00000409883.7:c.1054del MANE Select	ENSP00000386264.2:p.Glu352AsnfsTer10
ENST00000286196.9:c.*618del	ENSP00000286196.5:n.*618del
ENST00000409444.6:c.1030del	ENSP00000387203.2:p.Glu344AsnfsTer10
ENST00000409883.6:c.1054del	ENSP00000386264.2:p.Glu352AsnfsTer10
ENST00000471318.5:n.282del
ENST00000495329.1:n.193del
ENST00000621467.4:c.1030del	ENSP00000480508.1:p.Glu344AsnfsTer10
NM_001044385.2:c.1054del	NP_001037850.1:p.Glu352AsnfsTer10
NM_152388.3:c.1030del	NP_689601.2:p.Glu344AsnfsTer10
NM_001044385.3:c.1054del MANE Select	NP_001037850.1:p.Glu352AsnfsTer10
NM_152388.4:c.1030del	NP_689601.2:p.Glu344AsnfsTer10