Canonical Allele Identifier: CA763362860

Gene: TMEM237

Linked Data

• dbSNP Id: rs1450930065
• MyVariant Identifiers: chr2:g.202491190_202491191del (hg19) ; chr2:g.201626467_201626468del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626468_201626469del , CM000664.2:g.201626468_201626469del	GRCh38
NC_000002.11:g.202491191_202491192del , CM000664.1:g.202491191_202491192del	GRCh37
NC_000002.10:g.202199436_202199437del	NCBI36
NG_032049.1:g.22062_22063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-321_834-320del
ENST00000621467.5:c.912-321_912-320del	ENSP00000480508.2:n.912-321_912-320del
ENST00000686475.1:n.978-321_978-320del
ENST00000409883.7:c.1038-321_1038-320del MANE Select	ENSP00000386264.2:n.1038-321_1038-320del
ENST00000286196.9:c.*602-321_*602-320del	ENSP00000286196.5:n.*602-321_*602-320del
ENST00000409444.6:c.1014-321_1014-320del	ENSP00000387203.2:n.1014-321_1014-320del
ENST00000409883.6:c.1038-321_1038-320del	ENSP00000386264.2:n.1038-321_1038-320del
ENST00000471318.5:n.266-321_266-320del
ENST00000621467.4:c.1014-321_1014-320del	ENSP00000480508.1:n.1014-321_1014-320del
NM_001044385.2:c.1038-321_1038-320del	NP_001037850.1:n.1038-321_1038-320del
NM_152388.3:c.1014-321_1014-320del	NP_689601.2:n.1014-321_1014-320del
NM_001044385.3:c.1038-321_1038-320del MANE Select	NP_001037850.1:n.1038-321_1038-320del
NM_152388.4:c.1014-321_1014-320del	NP_689601.2:n.1014-321_1014-320del