Canonical Allele Identifier: CA1139667041
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 951388
ClinVar RCV Id: RCV001223289
dbSNP Id: rs1928388987

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100407189del , CM000685.2:g.100407189del GRCh38
NC_000023.10:g.99662187del , CM000685.1:g.99662187del GRCh37
NC_000023.9:g.99548843del NCBI36
NG_021319.1:g.8086del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255531.8:c.1410del ENSP00000255531.7:p.Tyr471IlefsTer?
ENST00000373034.8:c.1410del MANE Select ENSP00000362125.4:p.Tyr471IlefsTer?
ENST00000420881.6:c.1410del ENSP00000400327.2:p.Tyr471IlefsTer?
NM_001105243.1:c.1410del NP_001098713.1:p.Tyr471IlefsTer?
NM_001184880.1:c.1410del NP_001171809.1:p.Tyr471IlefsTer?
NM_020766.2:c.1410del NP_065817.2:p.Tyr471IlefsTer?
XM_011530997.1:c.1410del XP_011529299.1:p.Tyr471IlefsTer?
XM_011530997.2:c.1410del XP_011529299.1:p.Tyr471IlefsTer?
NM_001105243.2:c.1410del NP_001098713.1:p.Tyr471IlefsTer?
NM_001184880.2:c.1410del MANE Select NP_001171809.1:p.Tyr471IlefsTer?
NM_020766.3:c.1410del NP_065817.2:p.Tyr471IlefsTer?