Canonical Allele Identifier: CA430649154

Gene: TMEM237 ENO1P4

Linked Data

• MyVariant Identifiers: chr2:g.202486913A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201622190A>C , CM000664.2:g.201622190A>C	GRCh38
NC_000002.11:g.202486913A>C , CM000664.1:g.202486913A>C	GRCh37
NC_000002.10:g.202195158A>C	NCBI36
NG_032049.1:g.26340T>G
NG_051007.1:g.1993T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*2065T>G (TMEM237)	ENSP00000480508.2:n.*2065T>G
ENST00000686475.1:n.3232T>G (TMEM237)
ENST00000409883.7:c.*2065T>G (TMEM237) MANE Select	ENSP00000386264.2:n.*2065T>G
ENST00000409444.6:c.*2065T>G (TMEM237)	ENSP00000387203.2:n.*2065T>G
ENST00000409883.6:c.*2065T>G (TMEM237)	ENSP00000386264.2:n.*2065T>G
ENST00000416471.2:n.1241T>G (ENO1P4)
ENST00000495329.1:n.2431T>G (TMEM237)
NM_001044385.2:c.*2065T>G (TMEM237)	NP_001037850.1:n.*2065T>G
NM_152388.3:c.*2065T>G (TMEM237)	NP_689601.2:n.*2065T>G
NM_001044385.3:c.*2065T>G (TMEM237) MANE Select	NP_001037850.1:n.*2065T>G
NM_152388.4:c.*2065T>G (TMEM237)	NP_689601.2:n.*2065T>G