Canonical Allele Identifier: CA350304399

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490791A>T (hg19) ; chr2:g.201626068A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626068A>T , CM000664.2:g.201626068A>T	GRCh38
NC_000002.11:g.202490791A>T , CM000664.1:g.202490791A>T	GRCh37
NC_000002.10:g.202199036A>T	NCBI36
NG_032049.1:g.22462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.913T>A
ENST00000621467.5:c.991T>A	ENSP00000480508.2:p.Trp331Arg
ENST00000686475.1:n.1057T>A
ENST00000409883.7:c.1117T>A MANE Select	ENSP00000386264.2:p.Trp373Arg
ENST00000286196.9:c.*681T>A	ENSP00000286196.5:n.*681T>A
ENST00000409444.6:c.1093T>A	ENSP00000387203.2:p.Trp365Arg
ENST00000409883.6:c.1117T>A	ENSP00000386264.2:p.Trp373Arg
ENST00000471318.5:n.345T>A
ENST00000495329.1:n.256T>A
ENST00000621467.4:c.1093T>A	ENSP00000480508.1:p.Trp365Arg
NM_001044385.2:c.1117T>A	NP_001037850.1:p.Trp373Arg
NM_152388.3:c.1093T>A	NP_689601.2:p.Trp365Arg
NM_001044385.3:c.1117T>A MANE Select	NP_001037850.1:p.Trp373Arg
NM_152388.4:c.1093T>A	NP_689601.2:p.Trp365Arg