Canonical Allele Identifier: CA2753880766

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623467A>T , CM000664.2:g.201623467A>T	GRCh38
NC_000002.11:g.202488190A>T , CM000664.1:g.202488190A>T	GRCh37
NC_000002.10:g.202196435A>T	NCBI36
NG_032049.1:g.25063T>A
NG_051007.1:g.716T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*788T>A	ENSP00000480508.2:n.*788T>A
ENST00000686475.1:n.1955T>A
ENST00000409883.7:c.*788T>A MANE Select	ENSP00000386264.2:n.*788T>A
ENST00000409444.6:c.*788T>A	ENSP00000387203.2:n.*788T>A
ENST00000409883.6:c.*788T>A	ENSP00000386264.2:n.*788T>A
ENST00000495329.1:n.1154T>A
NM_001044385.2:c.*788T>A	NP_001037850.1:n.*788T>A
NM_152388.3:c.*788T>A	NP_689601.2:n.*788T>A
NM_001044385.3:c.*788T>A MANE Select	NP_001037850.1:n.*788T>A
NM_152388.4:c.*788T>A	NP_689601.2:n.*788T>A