Canonical Allele Identifier: CA517748616

Gene: PCDH19

Linked Data

• gnomAD v4: X-100407692-G-T
• MyVariant Identifiers: chrX:g.99662690G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100407692G>T , CM000685.2:g.100407692G>T	GRCh38
NC_000023.10:g.99662690G>T , CM000685.1:g.99662690G>T	GRCh37
NC_000023.9:g.99549346G>T	NCBI36
NG_021319.1:g.7582C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255531.8:c.906C>A	ENSP00000255531.7:p.Gly302=
ENST00000373034.8:c.906C>A MANE Select	ENSP00000362125.4:p.Gly302=
ENST00000420881.6:c.906C>A	ENSP00000400327.2:p.Gly302=
NM_001105243.1:c.906C>A	NP_001098713.1:p.Gly302=
NM_001184880.1:c.906C>A	NP_001171809.1:p.Gly302=
NM_020766.2:c.906C>A	NP_065817.2:p.Gly302=
XM_011530997.1:c.906C>A	XP_011529299.1:p.Gly302=
XM_011530997.2:c.906C>A	XP_011529299.1:p.Gly302=
NM_001105243.2:c.906C>A	NP_001098713.1:p.Gly302=
NM_001184880.2:c.906C>A MANE Select	NP_001171809.1:p.Gly302=
NM_020766.3:c.906C>A	NP_065817.2:p.Gly302=