Canonical Allele Identifier: CA538945384

Gene: TMEM237

Linked Data

• dbSNP Id: rs1160133548
• gnomAD v2: 2-202488186-G-GA
• gnomAD v4: 2-201623463-G-GA
• MyVariant Identifiers: chr2:g.202488186_202488187insA (hg19) ; chr2:g.201623463_201623464insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623469dup , CM000664.2:g.201623469dup	GRCh38
NC_000002.11:g.202488192dup , CM000664.1:g.202488192dup	GRCh37
NC_000002.10:g.202196437dup	NCBI36
NG_032049.1:g.25066dup
NG_051007.1:g.719dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*791dup	ENSP00000480508.2:n.*791dup
ENST00000686475.1:n.1958dup
ENST00000409883.7:c.*791dup MANE Select	ENSP00000386264.2:n.*791dup
ENST00000409444.6:c.*791dup	ENSP00000387203.2:n.*791dup
ENST00000409883.6:c.*791dup	ENSP00000386264.2:n.*791dup
ENST00000495329.1:n.1157dup
NM_001044385.2:c.*791dup	NP_001037850.1:n.*791dup
NM_152388.3:c.*791dup	NP_689601.2:n.*791dup
NM_001044385.3:c.*791dup MANE Select	NP_001037850.1:n.*791dup
NM_152388.4:c.*791dup	NP_689601.2:n.*791dup