Canonical Allele Identifier: CA414000148
Gene: PCDH19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.100342022T>G , CM000685.2:g.100342022T>G GRCh38
NC_000023.10:g.99597020T>G , CM000685.1:g.99597020T>G GRCh37
NC_000023.9:g.99483676T>G NCBI36
NG_021319.1:g.73252A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255531.8:c.2588A>C ENSP00000255531.7:p.Glu863Ala
ENST00000373034.8:c.2729A>C MANE Select ENSP00000362125.4:p.Glu910Ala
ENST00000420881.6:c.2585A>C ENSP00000400327.2:p.Glu862Ala
NM_001105243.1:c.2588A>C NP_001098713.1:p.Glu863Ala
NM_001184880.1:c.2729A>C NP_001171809.1:p.Glu910Ala
NM_020766.2:c.2585A>C NP_065817.2:p.Glu862Ala
XM_011530997.1:c.2726A>C XP_011529299.1:p.Glu909Ala
XM_011530997.2:c.2726A>C XP_011529299.1:p.Glu909Ala
NM_001105243.2:c.2588A>C NP_001098713.1:p.Glu863Ala
NM_001184880.2:c.2729A>C MANE Select NP_001171809.1:p.Glu910Ala
NM_020766.3:c.2585A>C NP_065817.2:p.Glu862Ala