Canonical Allele Identifier: CA2662657718

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626433-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626433A>C , CM000664.2:g.201626433A>C	GRCh38
NC_000002.11:g.202491156A>C , CM000664.1:g.202491156A>C	GRCh37
NC_000002.10:g.202199401A>C	NCBI36
NG_032049.1:g.22097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-286T>G
ENST00000621467.5:c.912-286T>G	ENSP00000480508.2:n.912-286T>G
ENST00000686475.1:n.978-286T>G
ENST00000409883.7:c.1038-286T>G MANE Select	ENSP00000386264.2:n.1038-286T>G
ENST00000286196.9:c.*602-286T>G	ENSP00000286196.5:n.*602-286T>G
ENST00000409444.6:c.1014-286T>G	ENSP00000387203.2:n.1014-286T>G
ENST00000409883.6:c.1038-286T>G	ENSP00000386264.2:n.1038-286T>G
ENST00000471318.5:n.266-286T>G
ENST00000621467.4:c.1014-286T>G	ENSP00000480508.1:n.1014-286T>G
NM_001044385.2:c.1038-286T>G	NP_001037850.1:n.1038-286T>G
NM_152388.3:c.1014-286T>G	NP_689601.2:n.1014-286T>G
NM_001044385.3:c.1038-286T>G MANE Select	NP_001037850.1:n.1038-286T>G
NM_152388.4:c.1014-286T>G	NP_689601.2:n.1014-286T>G