Canonical Allele Identifier: CA2662656970

Gene: TMEM237 ENO1P4

Linked Data

• gnomAD v4: 2-201623326-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623328del , CM000664.2:g.201623328del	GRCh38
NC_000002.11:g.202488051del , CM000664.1:g.202488051del	GRCh37
NC_000002.10:g.202196296del	NCBI36
NG_032049.1:g.25203del
NG_051007.1:g.856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*928del (TMEM237)	ENSP00000480508.2:n.*928del
ENST00000686475.1:n.2095del (TMEM237)
ENST00000409883.7:c.*928del (TMEM237) MANE Select	ENSP00000386264.2:n.*928del
ENST00000409444.6:c.*928del (TMEM237)	ENSP00000387203.2:n.*928del
ENST00000409883.6:c.*928del (TMEM237)	ENSP00000386264.2:n.*928del
ENST00000416471.2:n.104del (ENO1P4)
ENST00000495329.1:n.1294del (TMEM237)
NM_001044385.2:c.*928del (TMEM237)	NP_001037850.1:n.*928del
NM_152388.3:c.*928del (TMEM237)	NP_689601.2:n.*928del
NM_001044385.3:c.*928del (TMEM237) MANE Select	NP_001037850.1:n.*928del
NM_152388.4:c.*928del (TMEM237)	NP_689601.2:n.*928del