Canonical Allele Identifier: CA2662657026

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201623491-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623493_201623494del , CM000664.2:g.201623493_201623494del	GRCh38
NC_000002.11:g.202488216_202488217del , CM000664.1:g.202488216_202488217del	GRCh37
NC_000002.10:g.202196461_202196462del	NCBI36
NG_032049.1:g.25037_25038del
NG_051007.1:g.690_691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*762_*763del	ENSP00000480508.2:n.*762_*763del
ENST00000686475.1:n.1929_1930del
ENST00000409883.7:c.*762_*763del MANE Select	ENSP00000386264.2:n.*762_*763del
ENST00000409444.6:c.*762_*763del	ENSP00000387203.2:n.*762_*763del
ENST00000409883.6:c.*762_*763del	ENSP00000386264.2:n.*762_*763del
ENST00000495329.1:n.1128_1129del
NM_001044385.2:c.*762_*763del	NP_001037850.1:n.*762_*763del
NM_152388.3:c.*762_*763del	NP_689601.2:n.*762_*763del
NM_001044385.3:c.*762_*763del MANE Select	NP_001037850.1:n.*762_*763del
NM_152388.4:c.*762_*763del	NP_689601.2:n.*762_*763del