Canonical Allele Identifier: CA10468944

Gene: PCDH19

Linked Data

• ClinVar Variation Id: 465311
• ClinVar RCV Id: RCV000538675
• dbSNP Id: rs779759129
• ExAC: X:99662738 G / A
• gnomAD v2: X-99662738-G-A
• gnomAD v4: X-100407740-G-A
• MyVariant Identifiers: chrX:g.99662738G>A (hg19) ; chrX:g.100407740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100407740G>A , CM000685.2:g.100407740G>A	GRCh38
NC_000023.10:g.99662738G>A , CM000685.1:g.99662738G>A	GRCh37
NC_000023.9:g.99549394G>A	NCBI36
NG_021319.1:g.7534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.858C>T	ENSP00000255531.7:p.Arg286=
ENST00000373034.8:c.858C>T MANE Select	ENSP00000362125.4:p.Arg286=
ENST00000420881.6:c.858C>T	ENSP00000400327.2:p.Arg286=
NM_001105243.1:c.858C>T	NP_001098713.1:p.Arg286=
NM_001184880.1:c.858C>T	NP_001171809.1:p.Arg286=
NM_020766.2:c.858C>T	NP_065817.2:p.Arg286=
XM_011530997.1:c.858C>T	XP_011529299.1:p.Arg286=
XM_011530997.2:c.858C>T	XP_011529299.1:p.Arg286=
NM_001105243.2:c.858C>T	NP_001098713.1:p.Arg286=
NM_001184880.2:c.858C>T MANE Select	NP_001171809.1:p.Arg286=
NM_020766.3:c.858C>T	NP_065817.2:p.Arg286=