Canonical Allele Identifier: CA517747555

Gene: PCDH19

Linked Data

• ClinVar Variation Id: 2726579
• ClinVar RCV Id: RCV003511224
• gnomAD v4: X-100406896-G-A
• MyVariant Identifiers: chrX:g.99661894G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100406896G>A , CM000685.2:g.100406896G>A	GRCh38
NC_000023.10:g.99661894G>A , CM000685.1:g.99661894G>A	GRCh37
NC_000023.9:g.99548550G>A	NCBI36
NG_021319.1:g.8378C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.1702C>T	ENSP00000255531.7:p.Leu568=
ENST00000373034.8:c.1702C>T MANE Select	ENSP00000362125.4:p.Leu568=
ENST00000420881.6:c.1702C>T	ENSP00000400327.2:p.Leu568=
NM_001105243.1:c.1702C>T	NP_001098713.1:p.Leu568=
NM_001184880.1:c.1702C>T	NP_001171809.1:p.Leu568=
NM_020766.2:c.1702C>T	NP_065817.2:p.Leu568=
XM_011530997.1:c.1702C>T	XP_011529299.1:p.Leu568=
XM_011530997.2:c.1702C>T	XP_011529299.1:p.Leu568=
NM_001105243.2:c.1702C>T	NP_001098713.1:p.Leu568=
NM_001184880.2:c.1702C>T MANE Select	NP_001171809.1:p.Leu568=
NM_020766.3:c.1702C>T	NP_065817.2:p.Leu568=