Canonical Allele Identifier: CA2565267703
Gene: PCDH19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100407461_100407467del , CM000685.2:g.100407461_100407467del GRCh38
NC_000023.10:g.99662459_99662465del , CM000685.1:g.99662459_99662465del GRCh37
NC_000023.9:g.99549115_99549121del NCBI36
NG_021319.1:g.7811_7817del

Transcript Alleles

HGVS Amino-acid change
ENST00000255531.8:c.1135_1141del ENSP00000255531.7:p.Gly379MetfsTer?
ENST00000373034.8:c.1135_1141del MANE Select ENSP00000362125.4:p.Gly379MetfsTer?
ENST00000420881.6:c.1135_1141del ENSP00000400327.2:p.Gly379MetfsTer?
NM_001105243.1:c.1135_1141del NP_001098713.1:p.Gly379MetfsTer?
NM_001184880.1:c.1135_1141del NP_001171809.1:p.Gly379MetfsTer?
NM_020766.2:c.1135_1141del NP_065817.2:p.Gly379MetfsTer?
XM_011530997.1:c.1135_1141del XP_011529299.1:p.Gly379MetfsTer?
XM_011530997.2:c.1135_1141del XP_011529299.1:p.Gly379MetfsTer?
NM_001105243.2:c.1135_1141del NP_001098713.1:p.Gly379MetfsTer?
NM_001184880.2:c.1135_1141del MANE Select NP_001171809.1:p.Gly379MetfsTer?
NM_020766.3:c.1135_1141del NP_065817.2:p.Gly379MetfsTer?