Canonical Allele Identifier: CA2662657021

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201623474-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623474C>A , CM000664.2:g.201623474C>A	GRCh38
NC_000002.11:g.202488197C>A , CM000664.1:g.202488197C>A	GRCh37
NC_000002.10:g.202196442C>A	NCBI36
NG_032049.1:g.25056G>T
NG_051007.1:g.709G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*781G>T	ENSP00000480508.2:n.*781G>T
ENST00000686475.1:n.1948G>T
ENST00000409883.7:c.*781G>T MANE Select	ENSP00000386264.2:n.*781G>T
ENST00000409444.6:c.*781G>T	ENSP00000387203.2:n.*781G>T
ENST00000409883.6:c.*781G>T	ENSP00000386264.2:n.*781G>T
ENST00000495329.1:n.1147G>T
NM_001044385.2:c.*781G>T	NP_001037850.1:n.*781G>T
NM_152388.3:c.*781G>T	NP_689601.2:n.*781G>T
NM_001044385.3:c.*781G>T MANE Select	NP_001037850.1:n.*781G>T
NM_152388.4:c.*781G>T	NP_689601.2:n.*781G>T