Canonical Allele Identifier: CA2630293109
Gene: MESP2 HGNC NCBI

Linked Data

gnomAD v4: 15-89776824-CG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776828del , CM000677.2:g.89776828del GRCh38
NC_000015.9:g.90320059del , CM000677.1:g.90320059del GRCh37
NC_000015.8:g.88121063del NCBI36
NG_008608.1:g.5471del
NG_008608.2:g.21238del

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.471del MANE Select ENSP00000342392.3:p.Ser158ProfsTer?
ENST00000341735.3:c.471del ENSP00000342392.3:p.Ser158ProfsTer?
ENST00000558723.1:n.39-1237del
ENST00000560219.2:c.31-1237del ENSP00000452998.1:n.31-1237del
NM_001039958.1:c.471del NP_001035047.1:p.Ser158ProfsTer?
NM_001039958.2:c.471del MANE Select NP_001035047.1:p.Ser158ProfsTer?
Search 100 bp 5'
Search 100 bp 3'