Canonical Allele Identifier: CA1321143759

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957729569

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623530_201623532del , CM000664.2:g.201623530_201623532del	GRCh38
NC_000002.11:g.202488253_202488255del , CM000664.1:g.202488253_202488255del	GRCh37
NC_000002.10:g.202196498_202196500del	NCBI36
NG_032049.1:g.24998_25000del
NG_051007.1:g.651_653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*723_*725del	ENSP00000480508.2:n.*723_*725del
ENST00000686475.1:n.1890_1892del
ENST00000409883.7:c.*723_*725del MANE Select	ENSP00000386264.2:n.*723_*725del
ENST00000409444.6:c.*723_*725del	ENSP00000387203.2:n.*723_*725del
ENST00000409883.6:c.*723_*725del	ENSP00000386264.2:n.*723_*725del
ENST00000495329.1:n.1089_1091del
NM_001044385.2:c.*723_*725del	NP_001037850.1:n.*723_*725del
NM_152388.3:c.*723_*725del	NP_689601.2:n.*723_*725del
NM_001044385.3:c.*723_*725del MANE Select	NP_001037850.1:n.*723_*725del
NM_152388.4:c.*723_*725del	NP_689601.2:n.*723_*725del