Canonical Allele Identifier: CA430663034
Gene: TMEM237 HGNC NCBI
ENO1P4 HGNC NCBI

Linked Data

dbSNP Id: rs1957728098
MyVariant Identifiers: chr2:g.202488123C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623400C>A , CM000664.2:g.201623400C>A GRCh38
NC_000002.11:g.202488123C>A , CM000664.1:g.202488123C>A GRCh37
NC_000002.10:g.202196368C>A NCBI36
NG_032049.1:g.25130G>T
NG_051007.1:g.783G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*855G>T (TMEM237) ENSP00000480508.2:n.*855G>T
ENST00000686475.1:n.2022G>T (TMEM237)
ENST00000409883.7:c.*855G>T (TMEM237) MANE Select ENSP00000386264.2:n.*855G>T
ENST00000409444.6:c.*855G>T (TMEM237) ENSP00000387203.2:n.*855G>T
ENST00000409883.6:c.*855G>T (TMEM237) ENSP00000386264.2:n.*855G>T
ENST00000416471.2:n.31G>T (ENO1P4)
ENST00000495329.1:n.1221G>T (TMEM237)
NM_001044385.2:c.*855G>T (TMEM237) NP_001037850.1:n.*855G>T
NM_152388.3:c.*855G>T (TMEM237) NP_689601.2:n.*855G>T
NM_001044385.3:c.*855G>T (TMEM237) MANE Select NP_001037850.1:n.*855G>T
NM_152388.4:c.*855G>T (TMEM237) NP_689601.2:n.*855G>T
Search 100 bp 5'
Search 100 bp 3'