Canonical Allele Identifier: CA63949562

Gene: TMEM237 ENO1P4

Linked Data

• dbSNP Id: rs561043781
• MyVariant Identifiers: chr2:g.202488084G>T (hg19) ; chr2:g.201623361G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623361G>T , CM000664.2:g.201623361G>T	GRCh38
NC_000002.11:g.202488084G>T , CM000664.1:g.202488084G>T	GRCh37
NC_000002.10:g.202196329G>T	NCBI36
NG_032049.1:g.25169C>A
NG_051007.1:g.822C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*894C>A (TMEM237)	ENSP00000480508.2:n.*894C>A
ENST00000686475.1:n.2061C>A (TMEM237)
ENST00000409883.7:c.*894C>A (TMEM237) MANE Select	ENSP00000386264.2:n.*894C>A
ENST00000409444.6:c.*894C>A (TMEM237)	ENSP00000387203.2:n.*894C>A
ENST00000409883.6:c.*894C>A (TMEM237)	ENSP00000386264.2:n.*894C>A
ENST00000416471.2:n.70C>A (ENO1P4)
ENST00000495329.1:n.1260C>A (TMEM237)
NM_001044385.2:c.*894C>A (TMEM237)	NP_001037850.1:n.*894C>A
NM_152388.3:c.*894C>A (TMEM237)	NP_689601.2:n.*894C>A
NM_001044385.3:c.*894C>A (TMEM237) MANE Select	NP_001037850.1:n.*894C>A
NM_152388.4:c.*894C>A (TMEM237)	NP_689601.2:n.*894C>A