Canonical Allele Identifier: CA1321141651
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621210T= , CM000664.2:g.201621210T= GRCh38
NC_000002.11:g.202485933T= , CM000664.1:g.202485933T= GRCh37
NC_000002.10:g.202194178T= NCBI36
NG_032049.1:g.27320A=
NG_051007.1:g.2973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*3045A= ENSP00000480508.2:n.*3045A=
ENST00000686475.1:n.4212A=
ENST00000409883.7:c.*3045A= MANE Select ENSP00000386264.2:n.*3045A=
ENST00000409444.6:c.*3045A= ENSP00000387203.2:n.*3045A=
ENST00000409883.6:c.*3045A= ENSP00000386264.2:n.*3045A=
ENST00000495329.1:n.3411A=
NM_001044385.2:c.*3045A= NP_001037850.1:n.*3045A=
NM_152388.3:c.*3045A= NP_689601.2:n.*3045A=
NM_001044385.3:c.*3045A= MANE Select NP_001037850.1:n.*3045A=
NM_152388.4:c.*3045A= NP_689601.2:n.*3045A=