Canonical Allele Identifier: CA414000001

Gene: PCDH19

Linked Data

• MyVariant Identifiers: chrX:g.99596983C>G (hg19) ; chrX:g.100341985C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100341985C>G , CM000685.2:g.100341985C>G	GRCh38
NC_000023.10:g.99596983C>G , CM000685.1:g.99596983C>G	GRCh37
NC_000023.9:g.99483639C>G	NCBI36
NG_021319.1:g.73289G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255531.8:c.2625G>C	ENSP00000255531.7:p.Gln875His
ENST00000373034.8:c.2766G>C MANE Select	ENSP00000362125.4:p.Gln922His
ENST00000420881.6:c.2622G>C	ENSP00000400327.2:p.Gln874His
NM_001105243.1:c.2625G>C	NP_001098713.1:p.Gln875His
NM_001184880.1:c.2766G>C	NP_001171809.1:p.Gln922His
NM_020766.2:c.2622G>C	NP_065817.2:p.Gln874His
XM_011530997.1:c.2763G>C	XP_011529299.1:p.Gln921His
XM_011530997.2:c.2763G>C	XP_011529299.1:p.Gln921His
NM_001105243.2:c.2625G>C	NP_001098713.1:p.Gln875His
NM_001184880.2:c.2766G>C MANE Select	NP_001171809.1:p.Gln922His
NM_020766.3:c.2622G>C	NP_065817.2:p.Gln874His