Canonical Allele Identifier: CA1321141639
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621196_201621197delinsCA , CM000664.2:g.201621196_201621197delinsCA GRCh38
NC_000002.11:g.202485919_202485920delinsCA , CM000664.1:g.202485919_202485920delinsCA GRCh37
NC_000002.10:g.202194164_202194165delinsCA NCBI36
NG_032049.1:g.27333_27334delinsTG
NG_051007.1:g.2986_2987delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3058_*3059delinsTG ENSP00000480508.2:n.*3058_*3059delinsTG
ENST00000686475.1:n.4225_4226delinsTG
ENST00000409883.7:c.*3058_*3059delinsTG MANE Select ENSP00000386264.2:n.*3058_*3059delinsTG
ENST00000409444.6:c.*3058_*3059delinsTG ENSP00000387203.2:n.*3058_*3059delinsTG
ENST00000409883.6:c.*3058_*3059delinsTG ENSP00000386264.2:n.*3058_*3059delinsTG
ENST00000495329.1:n.3424_3425delinsTG
NM_001044385.2:c.*3058_*3059delinsTG NP_001037850.1:n.*3058_*3059delinsTG
NM_152388.3:c.*3058_*3059delinsTG NP_689601.2:n.*3058_*3059delinsTG
NM_001044385.3:c.*3058_*3059delinsTG MANE Select NP_001037850.1:n.*3058_*3059delinsTG
NM_152388.4:c.*3058_*3059delinsTG NP_689601.2:n.*3058_*3059delinsTG