Canonical Allele Identifier: CA414000155

Gene: PCDH19

Linked Data

• MyVariant Identifiers: chrX:g.99597022A>C (hg19) ; chrX:g.100342024A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100342024A>C , CM000685.2:g.100342024A>C	GRCh38
NC_000023.10:g.99597022A>C , CM000685.1:g.99597022A>C	GRCh37
NC_000023.9:g.99483678A>C	NCBI36
NG_021319.1:g.73250T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2586T>G	ENSP00000255531.7:p.His862Gln
ENST00000373034.8:c.2727T>G MANE Select	ENSP00000362125.4:p.His909Gln
ENST00000420881.6:c.2583T>G	ENSP00000400327.2:p.His861Gln
NM_001105243.1:c.2586T>G	NP_001098713.1:p.His862Gln
NM_001184880.1:c.2727T>G	NP_001171809.1:p.His909Gln
NM_020766.2:c.2583T>G	NP_065817.2:p.His861Gln
XM_011530997.1:c.2724T>G	XP_011529299.1:p.His908Gln
XM_011530997.2:c.2724T>G	XP_011529299.1:p.His908Gln
NM_001105243.2:c.2586T>G	NP_001098713.1:p.His862Gln
NM_001184880.2:c.2727T>G MANE Select	NP_001171809.1:p.His909Gln
NM_020766.3:c.2583T>G	NP_065817.2:p.His861Gln