Canonical Allele Identifier: CA2662659534

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201620820-T-TGACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201620820_201620821insGACAG , CM000664.2:g.201620820_201620821insGACAG	GRCh38
NC_000002.11:g.202485543_202485544insGACAG , CM000664.1:g.202485543_202485544insGACAG	GRCh37
NC_000002.10:g.202193788_202193789insGACAG	NCBI36
NG_032049.1:g.27709_27710insCTGTC
NG_051007.1:g.3362_3363insCTGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.*3434_*3435insCTGTC	ENSP00000480508.2:n.*3434_*3435insCTGTC
ENST00000686475.1:n.4601_4602insCTGTC
ENST00000409883.7:c.*3434_*3435insCTGTC MANE Select	ENSP00000386264.2:n.*3434_*3435insCTGTC
ENST00000409444.6:c.*3434_*3435insCTGTC	ENSP00000387203.2:n.*3434_*3435insCTGTC
ENST00000409883.6:c.*3434_*3435insCTGTC	ENSP00000386264.2:n.*3434_*3435insCTGTC
ENST00000495329.1:n.3800_3801insCTGTC
NM_001044385.2:c.*3434_*3435insCTGTC	NP_001037850.1:n.*3434_*3435insCTGTC
NM_152388.3:c.*3434_*3435insCTGTC	NP_689601.2:n.*3434_*3435insCTGTC
NM_001044385.3:c.*3434_*3435insCTGTC MANE Select	NP_001037850.1:n.*3434_*3435insCTGTC
NM_152388.4:c.*3434_*3435insCTGTC	NP_689601.2:n.*3434_*3435insCTGTC