Canonical Allele Identifier: CA763376089

Gene: TMEM237

Linked Data

• dbSNP Id: rs1456339258
• gnomAD v3: 2-201621140-TA-T
• gnomAD v4: 2-201621140-TA-T
• MyVariant Identifiers: chr2:g.202485864del (hg19) ; chr2:g.201621141del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201621142del , CM000664.2:g.201621142del	GRCh38
NC_000002.11:g.202485865del , CM000664.1:g.202485865del	GRCh37
NC_000002.10:g.202194110del	NCBI36
NG_032049.1:g.27389del
NG_051007.1:g.3042del

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.*3114del	ENSP00000480508.2:n.*3114del
ENST00000686475.1:n.4281del
ENST00000409883.7:c.*3114del MANE Select	ENSP00000386264.2:n.*3114del
ENST00000409444.6:c.*3114del	ENSP00000387203.2:n.*3114del
ENST00000409883.6:c.*3114del	ENSP00000386264.2:n.*3114del
ENST00000495329.1:n.3480del
NM_001044385.2:c.*3114del	NP_001037850.1:n.*3114del
NM_152388.3:c.*3114del	NP_689601.2:n.*3114del
NM_001044385.3:c.*3114del MANE Select	NP_001037850.1:n.*3114del
NM_152388.4:c.*3114del	NP_689601.2:n.*3114del