Canonical Allele Identifier: CA2607228910

Gene: TMEM237 ENO1P4

Linked Data

• gnomAD v3: 2-201623168-A-AT
• gnomAD v4: 2-201623168-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623168_201623169insT , CM000664.2:g.201623168_201623169insT	GRCh38
NC_000002.11:g.202487891_202487892insT , CM000664.1:g.202487891_202487892insT	GRCh37
NC_000002.10:g.202196136_202196137insT	NCBI36
NG_032049.1:g.25361_25362insA
NG_051007.1:g.1014_1015insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*1086_*1087insA (TMEM237)	ENSP00000480508.2:n.*1086_*1087insA
ENST00000686475.1:n.2253_2254insA (TMEM237)
ENST00000409883.7:c.*1086_*1087insA (TMEM237) MANE Select	ENSP00000386264.2:n.*1086_*1087insA
ENST00000409444.6:c.*1086_*1087insA (TMEM237)	ENSP00000387203.2:n.*1086_*1087insA
ENST00000409883.6:c.*1086_*1087insA (TMEM237)	ENSP00000386264.2:n.*1086_*1087insA
ENST00000416471.2:n.262_263insA (ENO1P4)
ENST00000495329.1:n.1452_1453insA (TMEM237)
NM_001044385.2:c.*1086_*1087insA (TMEM237)	NP_001037850.1:n.*1086_*1087insA
NM_152388.3:c.*1086_*1087insA (TMEM237)	NP_689601.2:n.*1086_*1087insA
NM_001044385.3:c.*1086_*1087insA (TMEM237) MANE Select	NP_001037850.1:n.*1086_*1087insA
NM_152388.4:c.*1086_*1087insA (TMEM237)	NP_689601.2:n.*1086_*1087insA