Canonical Allele Identifier: CA430664186

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490804C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626081C>G , CM000664.2:g.201626081C>G	GRCh38
NC_000002.11:g.202490804C>G , CM000664.1:g.202490804C>G	GRCh37
NC_000002.10:g.202199049C>G	NCBI36
NG_032049.1:g.22449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.900G>C
ENST00000621467.5:c.978G>C	ENSP00000480508.2:p.Leu326=
ENST00000686475.1:n.1044G>C
ENST00000409883.7:c.1104G>C MANE Select	ENSP00000386264.2:p.Leu368=
ENST00000286196.9:c.*668G>C	ENSP00000286196.5:n.*668G>C
ENST00000409444.6:c.1080G>C	ENSP00000387203.2:p.Leu360=
ENST00000409883.6:c.1104G>C	ENSP00000386264.2:p.Leu368=
ENST00000471318.5:n.332G>C
ENST00000495329.1:n.243G>C
ENST00000621467.4:c.1080G>C	ENSP00000480508.1:p.Leu360=
NM_001044385.2:c.1104G>C	NP_001037850.1:p.Leu368=
NM_152388.3:c.1080G>C	NP_689601.2:p.Leu360=
NM_001044385.3:c.1104G>C MANE Select	NP_001037850.1:p.Leu368=
NM_152388.4:c.1080G>C	NP_689601.2:p.Leu360=