Canonical Allele Identifier: CA2753881142

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626238_201626239insAGG , CM000664.2:g.201626238_201626239insAGG	GRCh38
NC_000002.11:g.202490961_202490962insAGG , CM000664.1:g.202490961_202490962insAGG	GRCh37
NC_000002.10:g.202199206_202199207insAGG	NCBI36
NG_032049.1:g.22291_22292insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-92_834-91insCCT
ENST00000621467.5:c.912-92_912-91insCCT	ENSP00000480508.2:n.912-92_912-91insCCT
ENST00000686475.1:n.978-92_978-91insCCT
ENST00000409883.7:c.1038-92_1038-91insCCT MANE Select	ENSP00000386264.2:n.1038-92_1038-91insCCT
ENST00000286196.9:c.*602-92_*602-91insCCT	ENSP00000286196.5:n.*602-92_*602-91insCCT
ENST00000409444.6:c.1014-92_1014-91insCCT	ENSP00000387203.2:n.1014-92_1014-91insCCT
ENST00000409883.6:c.1038-92_1038-91insCCT	ENSP00000386264.2:n.1038-92_1038-91insCCT
ENST00000471318.5:n.266-92_266-91insCCT
ENST00000495329.1:n.85_86insCCT
ENST00000621467.4:c.1014-92_1014-91insCCT	ENSP00000480508.1:n.1014-92_1014-91insCCT
NM_001044385.2:c.1038-92_1038-91insCCT	NP_001037850.1:n.1038-92_1038-91insCCT
NM_152388.3:c.1014-92_1014-91insCCT	NP_689601.2:n.1014-92_1014-91insCCT
NM_001044385.3:c.1038-92_1038-91insCCT MANE Select	NP_001037850.1:n.1038-92_1038-91insCCT
NM_152388.4:c.1014-92_1014-91insCCT	NP_689601.2:n.1014-92_1014-91insCCT