Canonical Allele Identifier: CA430648422

Gene: TMEM237 ENO1P4

Linked Data

• MyVariant Identifiers: chr2:g.202486852A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201622129A>T , CM000664.2:g.201622129A>T	GRCh38
NC_000002.11:g.202486852A>T , CM000664.1:g.202486852A>T	GRCh37
NC_000002.10:g.202195097A>T	NCBI36
NG_032049.1:g.26401T>A
NG_051007.1:g.2054T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*2126T>A (TMEM237)	ENSP00000480508.2:n.*2126T>A
ENST00000686475.1:n.3293T>A (TMEM237)
ENST00000409883.7:c.*2126T>A (TMEM237) MANE Select	ENSP00000386264.2:n.*2126T>A
ENST00000409444.6:c.*2126T>A (TMEM237)	ENSP00000387203.2:n.*2126T>A
ENST00000409883.6:c.*2126T>A (TMEM237)	ENSP00000386264.2:n.*2126T>A
ENST00000416471.2:n.1302T>A (ENO1P4)
ENST00000495329.1:n.2492T>A (TMEM237)
NM_001044385.2:c.*2126T>A (TMEM237)	NP_001037850.1:n.*2126T>A
NM_152388.3:c.*2126T>A (TMEM237)	NP_689601.2:n.*2126T>A
NM_001044385.3:c.*2126T>A (TMEM237) MANE Select	NP_001037850.1:n.*2126T>A
NM_152388.4:c.*2126T>A (TMEM237)	NP_689601.2:n.*2126T>A