Canonical Allele Identifier: CA430663991

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626048-C-T
• MyVariant Identifiers: chr2:g.202490771C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626048C>T , CM000664.2:g.201626048C>T	GRCh38
NC_000002.11:g.202490771C>T , CM000664.1:g.202490771C>T	GRCh37
NC_000002.10:g.202199016C>T	NCBI36
NG_032049.1:g.22482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.933G>A
ENST00000621467.5:c.1011G>A	ENSP00000480508.2:p.Arg337=
ENST00000686475.1:n.1077G>A
ENST00000409883.7:c.1137G>A MANE Select	ENSP00000386264.2:p.Arg379=
ENST00000286196.9:c.*701G>A	ENSP00000286196.5:n.*701G>A
ENST00000409444.6:c.1113G>A	ENSP00000387203.2:p.Arg371=
ENST00000409883.6:c.1137G>A	ENSP00000386264.2:p.Arg379=
ENST00000471318.5:n.365G>A
ENST00000495329.1:n.276G>A
ENST00000621467.4:c.1113G>A	ENSP00000480508.1:p.Arg371=
NM_001044385.2:c.1137G>A	NP_001037850.1:p.Arg379=
NM_152388.3:c.1113G>A	NP_689601.2:p.Arg371=
NM_001044385.3:c.1137G>A MANE Select	NP_001037850.1:p.Arg379=
NM_152388.4:c.1113G>A	NP_689601.2:p.Arg371=