Canonical Allele Identifier: CA2753881170

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626263_201626264del , CM000664.2:g.201626263_201626264del	GRCh38
NC_000002.11:g.202490986_202490987del , CM000664.1:g.202490986_202490987del	GRCh37
NC_000002.10:g.202199231_202199232del	NCBI36
NG_032049.1:g.22266_22267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-117_834-116del
ENST00000621467.5:c.912-117_912-116del	ENSP00000480508.2:n.912-117_912-116del
ENST00000686475.1:n.978-117_978-116del
ENST00000409883.7:c.1038-117_1038-116del MANE Select	ENSP00000386264.2:n.1038-117_1038-116del
ENST00000286196.9:c.*602-117_*602-116del	ENSP00000286196.5:n.*602-117_*602-116del
ENST00000409444.6:c.1014-117_1014-116del	ENSP00000387203.2:n.1014-117_1014-116del
ENST00000409883.6:c.1038-117_1038-116del	ENSP00000386264.2:n.1038-117_1038-116del
ENST00000471318.5:n.266-117_266-116del
ENST00000495329.1:n.60_61del
ENST00000621467.4:c.1014-117_1014-116del	ENSP00000480508.1:n.1014-117_1014-116del
NM_001044385.2:c.1038-117_1038-116del	NP_001037850.1:n.1038-117_1038-116del
NM_152388.3:c.1014-117_1014-116del	NP_689601.2:n.1014-117_1014-116del
NM_001044385.3:c.1038-117_1038-116del MANE Select	NP_001037850.1:n.1038-117_1038-116del
NM_152388.4:c.1014-117_1014-116del	NP_689601.2:n.1014-117_1014-116del