Canonical Allele Identifier: CA2662657680

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626355-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626356_201626357del , CM000664.2:g.201626356_201626357del	GRCh38
NC_000002.11:g.202491079_202491080del , CM000664.1:g.202491079_202491080del	GRCh37
NC_000002.10:g.202199324_202199325del	NCBI36
NG_032049.1:g.22173_22174del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-210_834-209del
ENST00000621467.5:c.912-210_912-209del	ENSP00000480508.2:n.912-210_912-209del
ENST00000686475.1:n.978-210_978-209del
ENST00000409883.7:c.1038-210_1038-209del MANE Select	ENSP00000386264.2:n.1038-210_1038-209del
ENST00000286196.9:c.*602-210_*602-209del	ENSP00000286196.5:n.*602-210_*602-209del
ENST00000409444.6:c.1014-210_1014-209del	ENSP00000387203.2:n.1014-210_1014-209del
ENST00000409883.6:c.1038-210_1038-209del	ENSP00000386264.2:n.1038-210_1038-209del
ENST00000471318.5:n.266-210_266-209del
ENST00000621467.4:c.1014-210_1014-209del	ENSP00000480508.1:n.1014-210_1014-209del
NM_001044385.2:c.1038-210_1038-209del	NP_001037850.1:n.1038-210_1038-209del
NM_152388.3:c.1014-210_1014-209del	NP_689601.2:n.1014-210_1014-209del
NM_001044385.3:c.1038-210_1038-209del MANE Select	NP_001037850.1:n.1038-210_1038-209del
NM_152388.4:c.1014-210_1014-209del	NP_689601.2:n.1014-210_1014-209del