Canonical Allele Identifier: CA2701421376

Gene: TMEM237

Linked Data

• ClinVar Variation Id: 2844082
• ClinVar RCV Id: RCV003644148
• dbSNP Id: rs2105897395

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626163C>T , CM000664.2:g.201626163C>T	GRCh38
NC_000002.11:g.202490886C>T , CM000664.1:g.202490886C>T	GRCh37
NC_000002.10:g.202199131C>T	NCBI36
NG_032049.1:g.22367G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-16G>A
ENST00000621467.5:c.912-16G>A	ENSP00000480508.2:n.912-16G>A
ENST00000686475.1:n.978-16G>A
ENST00000409883.7:c.1038-16G>A MANE Select	ENSP00000386264.2:n.1038-16G>A
ENST00000286196.9:c.*602-16G>A	ENSP00000286196.5:n.*602-16G>A
ENST00000409444.6:c.1014-16G>A	ENSP00000387203.2:n.1014-16G>A
ENST00000409883.6:c.1038-16G>A	ENSP00000386264.2:n.1038-16G>A
ENST00000471318.5:n.266-16G>A
ENST00000495329.1:n.161G>A
ENST00000621467.4:c.1014-16G>A	ENSP00000480508.1:n.1014-16G>A
NM_001044385.2:c.1038-16G>A	NP_001037850.1:n.1038-16G>A
NM_152388.3:c.1014-16G>A	NP_689601.2:n.1014-16G>A
NM_001044385.3:c.1038-16G>A MANE Select	NP_001037850.1:n.1038-16G>A
NM_152388.4:c.1014-16G>A	NP_689601.2:n.1014-16G>A