Canonical Allele Identifier: CA2701423824

Gene: TMEM237 ENO1P4

Linked Data

• dbSNP Id: rs2105895376

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201622240_201622242del , CM000664.2:g.201622240_201622242del	GRCh38
NC_000002.11:g.202486963_202486965del , CM000664.1:g.202486963_202486965del	GRCh37
NC_000002.10:g.202195208_202195210del	NCBI36
NG_032049.1:g.26288_26290del
NG_051007.1:g.1941_1943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*2013_*2015del (TMEM237)	ENSP00000480508.2:n.*2013_*2015del
ENST00000686475.1:n.3180_3182del (TMEM237)
ENST00000409883.7:c.*2013_*2015del (TMEM237) MANE Select	ENSP00000386264.2:n.*2013_*2015del
ENST00000409444.6:c.*2013_*2015del (TMEM237)	ENSP00000387203.2:n.*2013_*2015del
ENST00000409883.6:c.*2013_*2015del (TMEM237)	ENSP00000386264.2:n.*2013_*2015del
ENST00000416471.2:n.1189_1191del (ENO1P4)
ENST00000495329.1:n.2379_2381del (TMEM237)
NM_001044385.2:c.*2013_*2015del (TMEM237)	NP_001037850.1:n.*2013_*2015del
NM_152388.3:c.*2013_*2015del (TMEM237)	NP_689601.2:n.*2013_*2015del
NM_001044385.3:c.*2013_*2015del (TMEM237) MANE Select	NP_001037850.1:n.*2013_*2015del
NM_152388.4:c.*2013_*2015del (TMEM237)	NP_689601.2:n.*2013_*2015del