Canonical Allele Identifier: CA430664129

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490792A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626069A>T , CM000664.2:g.201626069A>T	GRCh38
NC_000002.11:g.202490792A>T , CM000664.1:g.202490792A>T	GRCh37
NC_000002.10:g.202199037A>T	NCBI36
NG_032049.1:g.22461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.912T>A
ENST00000621467.5:c.990T>A	ENSP00000480508.2:p.Ser330=
ENST00000686475.1:n.1056T>A
ENST00000409883.7:c.1116T>A MANE Select	ENSP00000386264.2:p.Ser372=
ENST00000286196.9:c.*680T>A	ENSP00000286196.5:n.*680T>A
ENST00000409444.6:c.1092T>A	ENSP00000387203.2:p.Ser364=
ENST00000409883.6:c.1116T>A	ENSP00000386264.2:p.Ser372=
ENST00000471318.5:n.344T>A
ENST00000495329.1:n.255T>A
ENST00000621467.4:c.1092T>A	ENSP00000480508.1:p.Ser364=
NM_001044385.2:c.1116T>A	NP_001037850.1:p.Ser372=
NM_152388.3:c.1092T>A	NP_689601.2:p.Ser364=
NM_001044385.3:c.1116T>A MANE Select	NP_001037850.1:p.Ser372=
NM_152388.4:c.1092T>A	NP_689601.2:p.Ser364=