Canonical Allele Identifier: CA1321143289

Gene: TMEM237 ENO1P4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623016_201623018delinsGAA , CM000664.2:g.201623016_201623018delinsGAA	GRCh38
NC_000002.11:g.202487739_202487741delinsGAA , CM000664.1:g.202487739_202487741delinsGAA	GRCh37
NC_000002.10:g.202195984_202195986delinsGAA	NCBI36
NG_032049.1:g.25512_25514delinsTTC
NG_051007.1:g.1165_1167delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*1237_*1239delinsTTC (TMEM237)	ENSP00000480508.2:n.*1237_*1239delinsTTC
ENST00000686475.1:n.2404_2406delinsTTC (TMEM237)
ENST00000409883.7:c.*1237_*1239delinsTTC (TMEM237) MANE Select	ENSP00000386264.2:n.*1237_*1239delinsTTC
ENST00000409444.6:c.*1237_*1239delinsTTC (TMEM237)	ENSP00000387203.2:n.*1237_*1239delinsTTC
ENST00000409883.6:c.*1237_*1239delinsTTC (TMEM237)	ENSP00000386264.2:n.*1237_*1239delinsTTC
ENST00000416471.2:n.413_415delinsTTC (ENO1P4)
ENST00000495329.1:n.1603_1605delinsTTC (TMEM237)
NM_001044385.2:c.*1237_*1239delinsTTC (TMEM237)	NP_001037850.1:n.*1237_*1239delinsTTC
NM_152388.3:c.*1237_*1239delinsTTC (TMEM237)	NP_689601.2:n.*1237_*1239delinsTTC
NM_001044385.3:c.*1237_*1239delinsTTC (TMEM237) MANE Select	NP_001037850.1:n.*1237_*1239delinsTTC
NM_152388.4:c.*1237_*1239delinsTTC (TMEM237)	NP_689601.2:n.*1237_*1239delinsTTC