Canonical Allele Identifier: CA2607228913

Gene: TMEM237 ENO1P4

Linked Data

• gnomAD v3: 2-201623180-T-TCAGG
• gnomAD v4: 2-201623180-T-TCAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623180_201623181insCAGG , CM000664.2:g.201623180_201623181insCAGG	GRCh38
NC_000002.11:g.202487903_202487904insCAGG , CM000664.1:g.202487903_202487904insCAGG	GRCh37
NC_000002.10:g.202196148_202196149insCAGG	NCBI36
NG_032049.1:g.25349_25350insCCTG
NG_051007.1:g.1002_1003insCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*1074_*1075insCCTG (TMEM237)	ENSP00000480508.2:n.*1074_*1075insCCTG
ENST00000686475.1:n.2241_2242insCCTG (TMEM237)
ENST00000409883.7:c.*1074_*1075insCCTG (TMEM237) MANE Select	ENSP00000386264.2:n.*1074_*1075insCCTG
ENST00000409444.6:c.*1074_*1075insCCTG (TMEM237)	ENSP00000387203.2:n.*1074_*1075insCCTG
ENST00000409883.6:c.*1074_*1075insCCTG (TMEM237)	ENSP00000386264.2:n.*1074_*1075insCCTG
ENST00000416471.2:n.250_251insCCTG (ENO1P4)
ENST00000495329.1:n.1440_1441insCCTG (TMEM237)
NM_001044385.2:c.*1074_*1075insCCTG (TMEM237)	NP_001037850.1:n.*1074_*1075insCCTG
NM_152388.3:c.*1074_*1075insCCTG (TMEM237)	NP_689601.2:n.*1074_*1075insCCTG
NM_001044385.3:c.*1074_*1075insCCTG (TMEM237) MANE Select	NP_001037850.1:n.*1074_*1075insCCTG
NM_152388.4:c.*1074_*1075insCCTG (TMEM237)	NP_689601.2:n.*1074_*1075insCCTG