Canonical Allele Identifier: CA350304268

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626050-T-C
• MyVariant Identifiers: chr2:g.202490773T>C (hg19) ; chr2:g.201626050T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626050T>C , CM000664.2:g.201626050T>C	GRCh38
NC_000002.11:g.202490773T>C , CM000664.1:g.202490773T>C	GRCh37
NC_000002.10:g.202199018T>C	NCBI36
NG_032049.1:g.22480A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.931A>G
ENST00000621467.5:c.1009A>G	ENSP00000480508.2:p.Arg337Gly
ENST00000686475.1:n.1075A>G
ENST00000409883.7:c.1135A>G MANE Select	ENSP00000386264.2:p.Arg379Gly
ENST00000286196.9:c.*699A>G	ENSP00000286196.5:n.*699A>G
ENST00000409444.6:c.1111A>G	ENSP00000387203.2:p.Arg371Gly
ENST00000409883.6:c.1135A>G	ENSP00000386264.2:p.Arg379Gly
ENST00000471318.5:n.363A>G
ENST00000495329.1:n.274A>G
ENST00000621467.4:c.1111A>G	ENSP00000480508.1:p.Arg371Gly
NM_001044385.2:c.1135A>G	NP_001037850.1:p.Arg379Gly
NM_152388.3:c.1111A>G	NP_689601.2:p.Arg371Gly
NM_001044385.3:c.1135A>G MANE Select	NP_001037850.1:p.Arg379Gly
NM_152388.4:c.1111A>G	NP_689601.2:p.Arg371Gly