Canonical Allele Identifier: CA1321143745
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623514A= , CM000664.2:g.201623514A= GRCh38
NC_000002.11:g.202488237A= , CM000664.1:g.202488237A= GRCh37
NC_000002.10:g.202196482A= NCBI36
NG_032049.1:g.25016T=
NG_051007.1:g.669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*741T= ENSP00000480508.2:n.*741T=
ENST00000686475.1:n.1908T=
ENST00000409883.7:c.*741T= MANE Select ENSP00000386264.2:n.*741T=
ENST00000409444.6:c.*741T= ENSP00000387203.2:n.*741T=
ENST00000409883.6:c.*741T= ENSP00000386264.2:n.*741T=
ENST00000495329.1:n.1107T=
NM_001044385.2:c.*741T= NP_001037850.1:n.*741T=
NM_152388.3:c.*741T= NP_689601.2:n.*741T=
NM_001044385.3:c.*741T= MANE Select NP_001037850.1:n.*741T=
NM_152388.4:c.*741T= NP_689601.2:n.*741T=