Canonical Allele Identifier: CA1321142541

Gene: TMEM237 ENO1P4

Linked Data

• dbSNP Id: rs1957714045

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201622165_201622168dup , CM000664.2:g.201622165_201622168dup	GRCh38
NC_000002.11:g.202486888_202486891dup , CM000664.1:g.202486888_202486891dup	GRCh37
NC_000002.10:g.202195133_202195136dup	NCBI36
NG_032049.1:g.26363_26366dup
NG_051007.1:g.2016_2019dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*2088_*2091dup (TMEM237)	ENSP00000480508.2:n.*2088_*2091dup
ENST00000686475.1:n.3255_3258dup (TMEM237)
ENST00000409883.7:c.*2088_*2091dup (TMEM237) MANE Select	ENSP00000386264.2:n.*2088_*2091dup
ENST00000409444.6:c.*2088_*2091dup (TMEM237)	ENSP00000387203.2:n.*2088_*2091dup
ENST00000409883.6:c.*2088_*2091dup (TMEM237)	ENSP00000386264.2:n.*2088_*2091dup
ENST00000416471.2:n.1264_1267dup (ENO1P4)
ENST00000495329.1:n.2454_2457dup (TMEM237)
NM_001044385.2:c.*2088_*2091dup (TMEM237)	NP_001037850.1:n.*2088_*2091dup
NM_152388.3:c.*2088_*2091dup (TMEM237)	NP_689601.2:n.*2088_*2091dup
NM_001044385.3:c.*2088_*2091dup (TMEM237) MANE Select	NP_001037850.1:n.*2088_*2091dup
NM_152388.4:c.*2088_*2091dup (TMEM237)	NP_689601.2:n.*2088_*2091dup