Canonical Allele Identifier: CA2753881149

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626241_201626242insACA , CM000664.2:g.201626241_201626242insACA	GRCh38
NC_000002.11:g.202490964_202490965insACA , CM000664.1:g.202490964_202490965insACA	GRCh37
NC_000002.10:g.202199209_202199210insACA	NCBI36
NG_032049.1:g.22288_22289insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-95_834-94insTGT
ENST00000621467.5:c.912-95_912-94insTGT	ENSP00000480508.2:n.912-95_912-94insTGT
ENST00000686475.1:n.978-95_978-94insTGT
ENST00000409883.7:c.1038-95_1038-94insTGT MANE Select	ENSP00000386264.2:n.1038-95_1038-94insTGT
ENST00000286196.9:c.*602-95_*602-94insTGT	ENSP00000286196.5:n.*602-95_*602-94insTGT
ENST00000409444.6:c.1014-95_1014-94insTGT	ENSP00000387203.2:n.1014-95_1014-94insTGT
ENST00000409883.6:c.1038-95_1038-94insTGT	ENSP00000386264.2:n.1038-95_1038-94insTGT
ENST00000471318.5:n.266-95_266-94insTGT
ENST00000495329.1:n.82_83insTGT
ENST00000621467.4:c.1014-95_1014-94insTGT	ENSP00000480508.1:n.1014-95_1014-94insTGT
NM_001044385.2:c.1038-95_1038-94insTGT	NP_001037850.1:n.1038-95_1038-94insTGT
NM_152388.3:c.1014-95_1014-94insTGT	NP_689601.2:n.1014-95_1014-94insTGT
NM_001044385.3:c.1038-95_1038-94insTGT MANE Select	NP_001037850.1:n.1038-95_1038-94insTGT
NM_152388.4:c.1014-95_1014-94insTGT	NP_689601.2:n.1014-95_1014-94insTGT