Canonical Allele Identifier: CA2753881173

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626268_201626271del , CM000664.2:g.201626268_201626271del	GRCh38
NC_000002.11:g.202490991_202490994del , CM000664.1:g.202490991_202490994del	GRCh37
NC_000002.10:g.202199236_202199239del	NCBI36
NG_032049.1:g.22260_22263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-123_834-120del
ENST00000621467.5:c.912-123_912-120del	ENSP00000480508.2:n.912-123_912-120del
ENST00000686475.1:n.978-123_978-120del
ENST00000409883.7:c.1038-123_1038-120del MANE Select	ENSP00000386264.2:n.1038-123_1038-120del
ENST00000286196.9:c.*602-123_*602-120del	ENSP00000286196.5:n.*602-123_*602-120del
ENST00000409444.6:c.1014-123_1014-120del	ENSP00000387203.2:n.1014-123_1014-120del
ENST00000409883.6:c.1038-123_1038-120del	ENSP00000386264.2:n.1038-123_1038-120del
ENST00000471318.5:n.266-123_266-120del
ENST00000495329.1:n.54_57del
ENST00000621467.4:c.1014-123_1014-120del	ENSP00000480508.1:n.1014-123_1014-120del
NM_001044385.2:c.1038-123_1038-120del	NP_001037850.1:n.1038-123_1038-120del
NM_152388.3:c.1014-123_1014-120del	NP_689601.2:n.1014-123_1014-120del
NM_001044385.3:c.1038-123_1038-120del MANE Select	NP_001037850.1:n.1038-123_1038-120del
NM_152388.4:c.1014-123_1014-120del	NP_689601.2:n.1014-123_1014-120del