Canonical Allele Identifier: CA1321145905
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626063T= , CM000664.2:g.201626063T= GRCh38
NC_000002.11:g.202490786T= , CM000664.1:g.202490786T= GRCh37
NC_000002.10:g.202199031T= NCBI36
NG_032049.1:g.22467A=

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.918A=
ENST00000621467.5:c.996A= ENSP00000480508.2:p.Leu332=
ENST00000686475.1:n.1062A=
ENST00000409883.7:c.1122A= MANE Select ENSP00000386264.2:p.Leu374=
ENST00000286196.9:c.*686A= ENSP00000286196.5:n.*686A=
ENST00000409444.6:c.1098A= ENSP00000387203.2:p.Leu366=
ENST00000409883.6:c.1122A= ENSP00000386264.2:p.Leu374=
ENST00000471318.5:n.350A=
ENST00000495329.1:n.261A=
ENST00000621467.4:c.1098A= ENSP00000480508.1:p.Leu366=
NM_001044385.2:c.1122A= NP_001037850.1:p.Leu374=
NM_152388.3:c.1098A= NP_689601.2:p.Leu366=
NM_001044385.3:c.1122A= MANE Select NP_001037850.1:p.Leu374=
NM_152388.4:c.1098A= NP_689601.2:p.Leu366=