Canonical Allele Identifier: CA316278

Gene: PCDH19

Linked Data

• ClinVar Variation Id: 206307
• ClinVar RCV Id: RCV000188342
• dbSNP Id: rs796052794
• gnomAD v4: X-100408507-C-A
• MyVariant Identifiers: chrX:g.99663505C>A (hg19) ; chrX:g.100408507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100408507C>A , CM000685.2:g.100408507C>A	GRCh38
NC_000023.10:g.99663505C>A , CM000685.1:g.99663505C>A	GRCh37
NC_000023.9:g.99550161C>A	NCBI36
NG_021319.1:g.6767G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255531.8:c.91G>T	ENSP00000255531.7:p.Glu31Ter
ENST00000373034.8:c.91G>T MANE Select	ENSP00000362125.4:p.Glu31Ter
ENST00000420881.6:c.91G>T	ENSP00000400327.2:p.Glu31Ter
NM_001105243.1:c.91G>T	NP_001098713.1:p.Glu31Ter
NM_001184880.1:c.91G>T	NP_001171809.1:p.Glu31Ter
NM_020766.2:c.91G>T	NP_065817.2:p.Glu31Ter
XM_011530997.1:c.91G>T	XP_011529299.1:p.Glu31Ter
XM_011530997.2:c.91G>T	XP_011529299.1:p.Glu31Ter
NM_001105243.2:c.91G>T	NP_001098713.1:p.Glu31Ter
NM_001184880.2:c.91G>T MANE Select	NP_001171809.1:p.Glu31Ter
NM_020766.3:c.91G>T	NP_065817.2:p.Glu31Ter