Canonical Allele Identifier: CA1321143260
Gene: TMEM237 HGNC NCBI
ENO1P4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201622998_201622999delinsAC , CM000664.2:g.201622998_201622999delinsAC GRCh38
NC_000002.11:g.202487721_202487722delinsAC , CM000664.1:g.202487721_202487722delinsAC GRCh37
NC_000002.10:g.202195966_202195967delinsAC NCBI36
NG_032049.1:g.25531_25532delinsGT
NG_051007.1:g.1184_1185delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*1256_*1257delinsGT (TMEM237) ENSP00000480508.2:n.*1256_*1257delinsGT
ENST00000686475.1:n.2423_2424delinsGT (TMEM237)
ENST00000409883.7:c.*1256_*1257delinsGT (TMEM237) MANE Select ENSP00000386264.2:n.*1256_*1257delinsGT
ENST00000409444.6:c.*1256_*1257delinsGT (TMEM237) ENSP00000387203.2:n.*1256_*1257delinsGT
ENST00000409883.6:c.*1256_*1257delinsGT (TMEM237) ENSP00000386264.2:n.*1256_*1257delinsGT
ENST00000416471.2:n.432_433delinsGT (ENO1P4)
ENST00000495329.1:n.1622_1623delinsGT (TMEM237)
NM_001044385.2:c.*1256_*1257delinsGT (TMEM237) NP_001037850.1:n.*1256_*1257delinsGT
NM_152388.3:c.*1256_*1257delinsGT (TMEM237) NP_689601.2:n.*1256_*1257delinsGT
NM_001044385.3:c.*1256_*1257delinsGT (TMEM237) MANE Select NP_001037850.1:n.*1256_*1257delinsGT
NM_152388.4:c.*1256_*1257delinsGT (TMEM237) NP_689601.2:n.*1256_*1257delinsGT