Canonical Allele Identifier: CA1321143541
Gene: TMEM237 HGNC NCBI
ENO1P4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623315T= , CM000664.2:g.201623315T= GRCh38
NC_000002.11:g.202488038T= , CM000664.1:g.202488038T= GRCh37
NC_000002.10:g.202196283T= NCBI36
NG_032049.1:g.25215A=
NG_051007.1:g.868A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*940A= (TMEM237) ENSP00000480508.2:n.*940A=
ENST00000686475.1:n.2107A= (TMEM237)
ENST00000409883.7:c.*940A= (TMEM237) MANE Select ENSP00000386264.2:n.*940A=
ENST00000409444.6:c.*940A= (TMEM237) ENSP00000387203.2:n.*940A=
ENST00000409883.6:c.*940A= (TMEM237) ENSP00000386264.2:n.*940A=
ENST00000416471.2:n.116A= (ENO1P4)
ENST00000495329.1:n.1306A= (TMEM237)
NM_001044385.2:c.*940A= (TMEM237) NP_001037850.1:n.*940A=
NM_152388.3:c.*940A= (TMEM237) NP_689601.2:n.*940A=
NM_001044385.3:c.*940A= (TMEM237) MANE Select NP_001037850.1:n.*940A=
NM_152388.4:c.*940A= (TMEM237) NP_689601.2:n.*940A=