Canonical Allele Identifier: CA430662535
Gene: TMEM237 HGNC NCBI
ENO1P4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.202488063A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623340A>T , CM000664.2:g.201623340A>T GRCh38
NC_000002.11:g.202488063A>T , CM000664.1:g.202488063A>T GRCh37
NC_000002.10:g.202196308A>T NCBI36
NG_032049.1:g.25190T>A
NG_051007.1:g.843T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*915T>A (TMEM237) ENSP00000480508.2:n.*915T>A
ENST00000686475.1:n.2082T>A (TMEM237)
ENST00000409883.7:c.*915T>A (TMEM237) MANE Select ENSP00000386264.2:n.*915T>A
ENST00000409444.6:c.*915T>A (TMEM237) ENSP00000387203.2:n.*915T>A
ENST00000409883.6:c.*915T>A (TMEM237) ENSP00000386264.2:n.*915T>A
ENST00000416471.2:n.91T>A (ENO1P4)
ENST00000495329.1:n.1281T>A (TMEM237)
NM_001044385.2:c.*915T>A (TMEM237) NP_001037850.1:n.*915T>A
NM_152388.3:c.*915T>A (TMEM237) NP_689601.2:n.*915T>A
NM_001044385.3:c.*915T>A (TMEM237) MANE Select NP_001037850.1:n.*915T>A
NM_152388.4:c.*915T>A (TMEM237) NP_689601.2:n.*915T>A
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