Canonical Allele Identifier: CA2753881155

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626242_201626243insAGT , CM000664.2:g.201626242_201626243insAGT	GRCh38
NC_000002.11:g.202490965_202490966insAGT , CM000664.1:g.202490965_202490966insAGT	GRCh37
NC_000002.10:g.202199210_202199211insAGT	NCBI36
NG_032049.1:g.22287_22288insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-96_834-95insACT
ENST00000621467.5:c.912-96_912-95insACT	ENSP00000480508.2:n.912-96_912-95insACT
ENST00000686475.1:n.978-96_978-95insACT
ENST00000409883.7:c.1038-96_1038-95insACT MANE Select	ENSP00000386264.2:n.1038-96_1038-95insACT
ENST00000286196.9:c.*602-96_*602-95insACT	ENSP00000286196.5:n.*602-96_*602-95insACT
ENST00000409444.6:c.1014-96_1014-95insACT	ENSP00000387203.2:n.1014-96_1014-95insACT
ENST00000409883.6:c.1038-96_1038-95insACT	ENSP00000386264.2:n.1038-96_1038-95insACT
ENST00000471318.5:n.266-96_266-95insACT
ENST00000495329.1:n.81_82insACT
ENST00000621467.4:c.1014-96_1014-95insACT	ENSP00000480508.1:n.1014-96_1014-95insACT
NM_001044385.2:c.1038-96_1038-95insACT	NP_001037850.1:n.1038-96_1038-95insACT
NM_152388.3:c.1014-96_1014-95insACT	NP_689601.2:n.1014-96_1014-95insACT
NM_001044385.3:c.1038-96_1038-95insACT MANE Select	NP_001037850.1:n.1038-96_1038-95insACT
NM_152388.4:c.1014-96_1014-95insACT	NP_689601.2:n.1014-96_1014-95insACT