Canonical Allele Identifier: CA1321141314
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201620802A= , CM000664.2:g.201620802A= GRCh38
NC_000002.11:g.202485525A= , CM000664.1:g.202485525A= GRCh37
NC_000002.10:g.202193770A= NCBI36
NG_032049.1:g.27728T=
NG_051007.1:g.3381T=

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3453T= ENSP00000480508.2:n.*3453T=
ENST00000686475.1:n.4620T=
ENST00000409883.7:c.*3453T= MANE Select ENSP00000386264.2:n.*3453T=
ENST00000409444.6:c.*3453T= ENSP00000387203.2:n.*3453T=
ENST00000409883.6:c.*3453T= ENSP00000386264.2:n.*3453T=
ENST00000495329.1:n.3819T=
NM_001044385.2:c.*3453T= NP_001037850.1:n.*3453T=
NM_152388.3:c.*3453T= NP_689601.2:n.*3453T=
NM_001044385.3:c.*3453T= MANE Select NP_001037850.1:n.*3453T=
NM_152388.4:c.*3453T= NP_689601.2:n.*3453T=