Canonical Allele Identifier: CA350304817

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490858A>C (hg19) ; chr2:g.201626135A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626135A>C , CM000664.2:g.201626135A>C	GRCh38
NC_000002.11:g.202490858A>C , CM000664.1:g.202490858A>C	GRCh37
NC_000002.10:g.202199103A>C	NCBI36
NG_032049.1:g.22395T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.846T>G
ENST00000621467.5:c.924T>G	ENSP00000480508.2:p.Ile308Met
ENST00000686475.1:n.990T>G
ENST00000409883.7:c.1050T>G MANE Select	ENSP00000386264.2:p.Ile350Met
ENST00000286196.9:c.*614T>G	ENSP00000286196.5:n.*614T>G
ENST00000409444.6:c.1026T>G	ENSP00000387203.2:p.Ile342Met
ENST00000409883.6:c.1050T>G	ENSP00000386264.2:p.Ile350Met
ENST00000471318.5:n.278T>G
ENST00000495329.1:n.189T>G
ENST00000621467.4:c.1026T>G	ENSP00000480508.1:p.Ile342Met
NM_001044385.2:c.1050T>G	NP_001037850.1:p.Ile350Met
NM_152388.3:c.1026T>G	NP_689601.2:p.Ile342Met
NM_001044385.3:c.1050T>G MANE Select	NP_001037850.1:p.Ile350Met
NM_152388.4:c.1026T>G	NP_689601.2:p.Ile342Met