Canonical Allele Identifier: CA2753881152

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626242_201626250del , CM000664.2:g.201626242_201626250del	GRCh38
NC_000002.11:g.202490965_202490973del , CM000664.1:g.202490965_202490973del	GRCh37
NC_000002.10:g.202199210_202199218del	NCBI36
NG_032049.1:g.22280_22288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-103_834-95del
ENST00000621467.5:c.912-103_912-95del	ENSP00000480508.2:n.912-103_912-95del
ENST00000686475.1:n.978-103_978-95del
ENST00000409883.7:c.1038-103_1038-95del MANE Select	ENSP00000386264.2:n.1038-103_1038-95del
ENST00000286196.9:c.*602-103_*602-95del	ENSP00000286196.5:n.*602-103_*602-95del
ENST00000409444.6:c.1014-103_1014-95del	ENSP00000387203.2:n.1014-103_1014-95del
ENST00000409883.6:c.1038-103_1038-95del	ENSP00000386264.2:n.1038-103_1038-95del
ENST00000471318.5:n.266-103_266-95del
ENST00000495329.1:n.74_82del
ENST00000621467.4:c.1014-103_1014-95del	ENSP00000480508.1:n.1014-103_1014-95del
NM_001044385.2:c.1038-103_1038-95del	NP_001037850.1:n.1038-103_1038-95del
NM_152388.3:c.1014-103_1014-95del	NP_689601.2:n.1014-103_1014-95del
NM_001044385.3:c.1038-103_1038-95del MANE Select	NP_001037850.1:n.1038-103_1038-95del
NM_152388.4:c.1014-103_1014-95del	NP_689601.2:n.1014-103_1014-95del