Canonical Allele Identifier: CA430662944

Gene: TMEM237 ENO1P4

Linked Data

• gnomAD v4: 2-201623387-G-T
• MyVariant Identifiers: chr2:g.202488110G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623387G>T , CM000664.2:g.201623387G>T	GRCh38
NC_000002.11:g.202488110G>T , CM000664.1:g.202488110G>T	GRCh37
NC_000002.10:g.202196355G>T	NCBI36
NG_032049.1:g.25143C>A
NG_051007.1:g.796C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*868C>A (TMEM237)	ENSP00000480508.2:n.*868C>A
ENST00000686475.1:n.2035C>A (TMEM237)
ENST00000409883.7:c.*868C>A (TMEM237) MANE Select	ENSP00000386264.2:n.*868C>A
ENST00000409444.6:c.*868C>A (TMEM237)	ENSP00000387203.2:n.*868C>A
ENST00000409883.6:c.*868C>A (TMEM237)	ENSP00000386264.2:n.*868C>A
ENST00000416471.2:n.44C>A (ENO1P4)
ENST00000495329.1:n.1234C>A (TMEM237)
NM_001044385.2:c.*868C>A (TMEM237)	NP_001037850.1:n.*868C>A
NM_152388.3:c.*868C>A (TMEM237)	NP_689601.2:n.*868C>A
NM_001044385.3:c.*868C>A (TMEM237) MANE Select	NP_001037850.1:n.*868C>A
NM_152388.4:c.*868C>A (TMEM237)	NP_689601.2:n.*868C>A