Canonical Allele Identifier: CA1321145903
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626062A= , CM000664.2:g.201626062A= GRCh38
NC_000002.11:g.202490785A= , CM000664.1:g.202490785A= GRCh37
NC_000002.10:g.202199030A= NCBI36
NG_032049.1:g.22468T=

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.919T=
ENST00000621467.5:c.997T= ENSP00000480508.2:p.Phe333=
ENST00000686475.1:n.1063T=
ENST00000409883.7:c.1123T= MANE Select ENSP00000386264.2:p.Phe375=
ENST00000286196.9:c.*687T= ENSP00000286196.5:n.*687T=
ENST00000409444.6:c.1099T= ENSP00000387203.2:p.Phe367=
ENST00000409883.6:c.1123T= ENSP00000386264.2:p.Phe375=
ENST00000471318.5:n.351T=
ENST00000495329.1:n.262T=
ENST00000621467.4:c.1099T= ENSP00000480508.1:p.Phe367=
NM_001044385.2:c.1123T= NP_001037850.1:p.Phe375=
NM_152388.3:c.1099T= NP_689601.2:p.Phe367=
NM_001044385.3:c.1123T= MANE Select NP_001037850.1:p.Phe375=
NM_152388.4:c.1099T= NP_689601.2:p.Phe367=