Canonical Allele Identifier: CA2753881168

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626262_201626263insACA , CM000664.2:g.201626262_201626263insACA	GRCh38
NC_000002.11:g.202490985_202490986insACA , CM000664.1:g.202490985_202490986insACA	GRCh37
NC_000002.10:g.202199230_202199231insACA	NCBI36
NG_032049.1:g.22267_22268insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-116_834-115insTGT
ENST00000621467.5:c.912-116_912-115insTGT	ENSP00000480508.2:n.912-116_912-115insTGT
ENST00000686475.1:n.978-116_978-115insTGT
ENST00000409883.7:c.1038-116_1038-115insTGT MANE Select	ENSP00000386264.2:n.1038-116_1038-115insTGT
ENST00000286196.9:c.*602-116_*602-115insTGT	ENSP00000286196.5:n.*602-116_*602-115insTGT
ENST00000409444.6:c.1014-116_1014-115insTGT	ENSP00000387203.2:n.1014-116_1014-115insTGT
ENST00000409883.6:c.1038-116_1038-115insTGT	ENSP00000386264.2:n.1038-116_1038-115insTGT
ENST00000471318.5:n.266-116_266-115insTGT
ENST00000495329.1:n.61_62insTGT
ENST00000621467.4:c.1014-116_1014-115insTGT	ENSP00000480508.1:n.1014-116_1014-115insTGT
NM_001044385.2:c.1038-116_1038-115insTGT	NP_001037850.1:n.1038-116_1038-115insTGT
NM_152388.3:c.1014-116_1014-115insTGT	NP_689601.2:n.1014-116_1014-115insTGT
NM_001044385.3:c.1038-116_1038-115insTGT MANE Select	NP_001037850.1:n.1038-116_1038-115insTGT
NM_152388.4:c.1014-116_1014-115insTGT	NP_689601.2:n.1014-116_1014-115insTGT