Canonical Allele Identifier: CA1321143370

Gene: TMEM237 ENO1P4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623102_201623103delinsCA , CM000664.2:g.201623102_201623103delinsCA	GRCh38
NC_000002.11:g.202487825_202487826delinsCA , CM000664.1:g.202487825_202487826delinsCA	GRCh37
NC_000002.10:g.202196070_202196071delinsCA	NCBI36
NG_032049.1:g.25427_25428delinsTG
NG_051007.1:g.1080_1081delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*1152_*1153delinsTG (TMEM237)	ENSP00000480508.2:n.*1152_*1153delinsTG
ENST00000686475.1:n.2319_2320delinsTG (TMEM237)
ENST00000409883.7:c.*1152_*1153delinsTG (TMEM237) MANE Select	ENSP00000386264.2:n.*1152_*1153delinsTG
ENST00000409444.6:c.*1152_*1153delinsTG (TMEM237)	ENSP00000387203.2:n.*1152_*1153delinsTG
ENST00000409883.6:c.*1152_*1153delinsTG (TMEM237)	ENSP00000386264.2:n.*1152_*1153delinsTG
ENST00000416471.2:n.328_329delinsTG (ENO1P4)
ENST00000495329.1:n.1518_1519delinsTG (TMEM237)
NM_001044385.2:c.*1152_*1153delinsTG (TMEM237)	NP_001037850.1:n.*1152_*1153delinsTG
NM_152388.3:c.*1152_*1153delinsTG (TMEM237)	NP_689601.2:n.*1152_*1153delinsTG
NM_001044385.3:c.*1152_*1153delinsTG (TMEM237) MANE Select	NP_001037850.1:n.*1152_*1153delinsTG
NM_152388.4:c.*1152_*1153delinsTG (TMEM237)	NP_689601.2:n.*1152_*1153delinsTG