Canonical Allele Identifier: CA350304601

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490826A>C (hg19) ; chr2:g.201626103A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626103A>C , CM000664.2:g.201626103A>C	GRCh38
NC_000002.11:g.202490826A>C , CM000664.1:g.202490826A>C	GRCh37
NC_000002.10:g.202199071A>C	NCBI36
NG_032049.1:g.22427T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.878T>G
ENST00000621467.5:c.956T>G	ENSP00000480508.2:p.Val319Gly
ENST00000686475.1:n.1022T>G
ENST00000409883.7:c.1082T>G MANE Select	ENSP00000386264.2:p.Val361Gly
ENST00000286196.9:c.*646T>G	ENSP00000286196.5:n.*646T>G
ENST00000409444.6:c.1058T>G	ENSP00000387203.2:p.Val353Gly
ENST00000409883.6:c.1082T>G	ENSP00000386264.2:p.Val361Gly
ENST00000471318.5:n.310T>G
ENST00000495329.1:n.221T>G
ENST00000621467.4:c.1058T>G	ENSP00000480508.1:p.Val353Gly
NM_001044385.2:c.1082T>G	NP_001037850.1:p.Val361Gly
NM_152388.3:c.1058T>G	NP_689601.2:p.Val353Gly
NM_001044385.3:c.1082T>G MANE Select	NP_001037850.1:p.Val361Gly
NM_152388.4:c.1058T>G	NP_689601.2:p.Val353Gly