Canonical Allele Identifier: CA350304309

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490779A>C (hg19) ; chr2:g.201626056A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626056A>C , CM000664.2:g.201626056A>C	GRCh38
NC_000002.11:g.202490779A>C , CM000664.1:g.202490779A>C	GRCh37
NC_000002.10:g.202199024A>C	NCBI36
NG_032049.1:g.22474T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.925T>G
ENST00000621467.5:c.1003T>G	ENSP00000480508.2:p.Ser335Ala
ENST00000686475.1:n.1069T>G
ENST00000409883.7:c.1129T>G MANE Select	ENSP00000386264.2:p.Ser377Ala
ENST00000286196.9:c.*693T>G	ENSP00000286196.5:n.*693T>G
ENST00000409444.6:c.1105T>G	ENSP00000387203.2:p.Ser369Ala
ENST00000409883.6:c.1129T>G	ENSP00000386264.2:p.Ser377Ala
ENST00000471318.5:n.357T>G
ENST00000495329.1:n.268T>G
ENST00000621467.4:c.1105T>G	ENSP00000480508.1:p.Ser369Ala
NM_001044385.2:c.1129T>G	NP_001037850.1:p.Ser377Ala
NM_152388.3:c.1105T>G	NP_689601.2:p.Ser369Ala
NM_001044385.3:c.1129T>G MANE Select	NP_001037850.1:p.Ser377Ala
NM_152388.4:c.1105T>G	NP_689601.2:p.Ser369Ala