Canonical Allele Identifier: CA1321143663
Gene: TMEM237 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623432G= , CM000664.2:g.201623432G= GRCh38
NC_000002.11:g.202488155G= , CM000664.1:g.202488155G= GRCh37
NC_000002.10:g.202196400G= NCBI36
NG_032049.1:g.25098C=
NG_051007.1:g.751C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*823C= ENSP00000480508.2:n.*823C=
ENST00000686475.1:n.1990C=
ENST00000409883.7:c.*823C= MANE Select ENSP00000386264.2:n.*823C=
ENST00000409444.6:c.*823C= ENSP00000387203.2:n.*823C=
ENST00000409883.6:c.*823C= ENSP00000386264.2:n.*823C=
ENST00000495329.1:n.1189C=
NM_001044385.2:c.*823C= NP_001037850.1:n.*823C=
NM_152388.3:c.*823C= NP_689601.2:n.*823C=
NM_001044385.3:c.*823C= MANE Select NP_001037850.1:n.*823C=
NM_152388.4:c.*823C= NP_689601.2:n.*823C=
Search 100 bp 5'
Search 100 bp 3'