Canonical Allele Identifier: CA350316549

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202504984C>G (hg19) ; chr2:g.201640261C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640261C>G , CM000664.2:g.201640261C>G	GRCh38
NC_000002.11:g.202504984C>G , CM000664.1:g.202504984C>G	GRCh37
NC_000002.10:g.202213229C>G	NCBI36
NG_032049.1:g.8269G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+632G>C	ENSP00000480508.2:n.-356+632G>C
ENST00000409883.7:c.79G>C MANE Select	ENSP00000386264.2:p.Asp27His
ENST00000286196.9:c.-1+632G>C	ENSP00000286196.5:n.-1+632G>C
ENST00000409444.6:c.55G>C	ENSP00000387203.2:p.Asp19His
ENST00000409883.6:c.79G>C	ENSP00000386264.2:p.Asp27His
ENST00000432684.6:c.79G>C	ENSP00000413230.2:p.Asp27His
ENST00000444047.6:c.79G>C	ENSP00000402681.2:p.Asp27His
ENST00000463205.2:n.82G>C
ENST00000489550.5:n.92+632G>C
ENST00000621467.4:c.50+632G>C	ENSP00000480508.1:n.50+632G>C
NM_001044385.2:c.79G>C	NP_001037850.1:p.Asp27His
NM_152388.3:c.55G>C	NP_689601.2:p.Asp19His
NM_001044385.3:c.79G>C MANE Select	NP_001037850.1:p.Asp27His
NM_152388.4:c.55G>C	NP_689601.2:p.Asp19His