Canonical Allele Identifier: CA121293
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 11016
ClinVar RCV Id: RCV000011763
dbSNP Id: rs132630323

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100407276A>T , CM000685.2:g.100407276A>T GRCh38
NC_000023.10:g.99662274A>T , CM000685.1:g.99662274A>T GRCh37
NC_000023.9:g.99548930A>T NCBI36
NG_021319.1:g.7998T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000255531.8:c.1322T>A ENSP00000255531.7:p.Val441Glu
ENST00000373034.8:c.1322T>A MANE Select ENSP00000362125.4:p.Val441Glu
ENST00000420881.6:c.1322T>A ENSP00000400327.2:p.Val441Glu
NM_001105243.1:c.1322T>A NP_001098713.1:p.Val441Glu
NM_001184880.1:c.1322T>A NP_001171809.1:p.Val441Glu
NM_020766.2:c.1322T>A NP_065817.2:p.Val441Glu
XM_011530997.1:c.1322T>A XP_011529299.1:p.Val441Glu
XM_011530997.2:c.1322T>A XP_011529299.1:p.Val441Glu
NM_001105243.2:c.1322T>A NP_001098713.1:p.Val441Glu
NM_001184880.2:c.1322T>A MANE Select NP_001171809.1:p.Val441Glu
NM_020766.3:c.1322T>A NP_065817.2:p.Val441Glu