Canonical Allele Identifier: CA2662657654

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626309-TATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626312_201626314del , CM000664.2:g.201626312_201626314del	GRCh38
NC_000002.11:g.202491035_202491037del , CM000664.1:g.202491035_202491037del	GRCh37
NC_000002.10:g.202199280_202199282del	NCBI36
NG_032049.1:g.22218_22220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-165_834-163del
ENST00000621467.5:c.912-165_912-163del	ENSP00000480508.2:n.912-165_912-163del
ENST00000686475.1:n.978-165_978-163del
ENST00000409883.7:c.1038-165_1038-163del MANE Select	ENSP00000386264.2:n.1038-165_1038-163del
ENST00000286196.9:c.*602-165_*602-163del	ENSP00000286196.5:n.*602-165_*602-163del
ENST00000409444.6:c.1014-165_1014-163del	ENSP00000387203.2:n.1014-165_1014-163del
ENST00000409883.6:c.1038-165_1038-163del	ENSP00000386264.2:n.1038-165_1038-163del
ENST00000471318.5:n.266-165_266-163del
ENST00000495329.1:n.12_14del
ENST00000621467.4:c.1014-165_1014-163del	ENSP00000480508.1:n.1014-165_1014-163del
NM_001044385.2:c.1038-165_1038-163del	NP_001037850.1:n.1038-165_1038-163del
NM_152388.3:c.1014-165_1014-163del	NP_689601.2:n.1014-165_1014-163del
NM_001044385.3:c.1038-165_1038-163del MANE Select	NP_001037850.1:n.1038-165_1038-163del
NM_152388.4:c.1014-165_1014-163del	NP_689601.2:n.1014-165_1014-163del