Canonical Allele Identifier: CA1139667041

Gene: PCDH19

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?