Canonical Allele Identifier: CA414002935

Gene: PCDH19

Linked Data

• ClinVar Variation Id: 975469
• ClinVar RCV Id: RCV001252103
• dbSNP Id: rs1928395285
• MyVariant Identifiers: chrX:g.99662253T>C (hg19) ; chrX:g.100407255T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100407255T>C , CM000685.2:g.100407255T>C	GRCh38
NC_000023.10:g.99662253T>C , CM000685.1:g.99662253T>C	GRCh37
NC_000023.9:g.99548909T>C	NCBI36
NG_021319.1:g.8019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.1343A>G	ENSP00000255531.7:p.Asp448Gly
ENST00000373034.8:c.1343A>G MANE Select	ENSP00000362125.4:p.Asp448Gly
ENST00000420881.6:c.1343A>G	ENSP00000400327.2:p.Asp448Gly
NM_001105243.1:c.1343A>G	NP_001098713.1:p.Asp448Gly
NM_001184880.1:c.1343A>G	NP_001171809.1:p.Asp448Gly
NM_020766.2:c.1343A>G	NP_065817.2:p.Asp448Gly
XM_011530997.1:c.1343A>G	XP_011529299.1:p.Asp448Gly
XM_011530997.2:c.1343A>G	XP_011529299.1:p.Asp448Gly
NM_001105243.2:c.1343A>G	NP_001098713.1:p.Asp448Gly
NM_001184880.2:c.1343A>G MANE Select	NP_001171809.1:p.Asp448Gly
NM_020766.3:c.1343A>G	NP_065817.2:p.Asp448Gly