Canonical Allele Identifier: CA2662656984
Gene: TMEM237 HGNC NCBI
ENO1P4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623379del , CM000664.2:g.201623379del GRCh38
NC_000002.11:g.202488102del , CM000664.1:g.202488102del GRCh37
NC_000002.10:g.202196347del NCBI36
NG_032049.1:g.25155del
NG_051007.1:g.808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*880del (TMEM237) ENSP00000480508.2:n.*880del
ENST00000686475.1:n.2047del (TMEM237)
ENST00000409883.7:c.*880del (TMEM237) MANE Select ENSP00000386264.2:n.*880del
ENST00000409444.6:c.*880del (TMEM237) ENSP00000387203.2:n.*880del
ENST00000409883.6:c.*880del (TMEM237) ENSP00000386264.2:n.*880del
ENST00000416471.2:n.56del (ENO1P4)
ENST00000495329.1:n.1246del (TMEM237)
NM_001044385.2:c.*880del (TMEM237) NP_001037850.1:n.*880del
NM_152388.3:c.*880del (TMEM237) NP_689601.2:n.*880del
NM_001044385.3:c.*880del (TMEM237) MANE Select NP_001037850.1:n.*880del
NM_152388.4:c.*880del (TMEM237) NP_689601.2:n.*880del