Canonical Allele Identifier: CA763362861

Gene: TMEM237

Linked Data

• dbSNP Id: rs1405723731
• gnomAD v4: 2-201626470-AC-A
• MyVariant Identifiers: chr2:g.202491194del (hg19) ; chr2:g.201626471del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626472del , CM000664.2:g.201626472del	GRCh38
NC_000002.11:g.202491195del , CM000664.1:g.202491195del	GRCh37
NC_000002.10:g.202199440del	NCBI36
NG_032049.1:g.22059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-324del
ENST00000621467.5:c.912-324del	ENSP00000480508.2:n.912-324del
ENST00000686475.1:n.978-324del
ENST00000409883.7:c.1038-324del MANE Select	ENSP00000386264.2:n.1038-324del
ENST00000286196.9:c.*602-324del	ENSP00000286196.5:n.*602-324del
ENST00000409444.6:c.1014-324del	ENSP00000387203.2:n.1014-324del
ENST00000409883.6:c.1038-324del	ENSP00000386264.2:n.1038-324del
ENST00000471318.5:n.266-324del
ENST00000621467.4:c.1014-324del	ENSP00000480508.1:n.1014-324del
NM_001044385.2:c.1038-324del	NP_001037850.1:n.1038-324del
NM_152388.3:c.1014-324del	NP_689601.2:n.1014-324del
NM_001044385.3:c.1038-324del MANE Select	NP_001037850.1:n.1038-324del
NM_152388.4:c.1014-324del	NP_689601.2:n.1014-324del