Canonical Allele Identifier: CA916083751
Gene: JAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 845971
ClinVar RCV Id: RCV001049155
dbSNP Id: rs2067394045

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10658632del , CM000682.2:g.10658632del GRCh38
NC_000020.10:g.10639280del , CM000682.1:g.10639280del GRCh37
NC_000020.9:g.10587280del NCBI36
NG_007496.1:g.20417del

Transcript Alleles

HGVS Amino-acid change
ENST00000254958.10:c.532del MANE Select ENSP00000254958.4:p.His178ThrfsTer8
ENST00000254958.9:c.532del ENSP00000254958.4:p.His178ThrfsTer8
ENST00000423891.6:n.398del
NM_000214.2:c.532del NP_000205.1:p.His178ThrfsTer8
NM_000214.3:c.532del MANE Select NP_000205.1:p.His178ThrfsTer8